Irritable Bowel SyndromePhase 2/3BC-IBSNCT07576634
Effects of Standardized Boswellia Carterii Extract on Irritable Bowel Syndrome Patients
A Phase 2/3 study testing Boswellia carterii Extract and Educationntal program for IBS patie in people with Irritable Bowel Syndrome, run by Mansoura University at 1 site in Egypt.
Trial summary
Irritable bowel syndrome (IBS) is a common condition that affects the stomach and intestines. It can cause abdominal pain, bloating, diarrhea, constipation, and changes in bowel habits, which may reduce a person's quality of life. Many people with IBS do not achieve complete symptom relief with standard treatments. Read more about this study
- Who is it for?
- Ages 18 to 65 years
- Conditions the study is for
- Irritable Bowel Syndrome
- What is being tested?
- Boswellia carterii Extract and Educationntal program for IBS patie
- Type of treatment
- Pill or oral medicine
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 60 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Jan 2025to 30 Jan 2026
- Phase
- Phase 2/3
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 65 years
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Adults diagnosed with irritable bowel syndrome (IBS) according to Rome III and Rome IV criteria Recurrent abdominal pain occurring at least once weekly during the preceding three months Presence of changes in stool frequency, stool form, or defecation associated with abdominal pain Participants reporting bloating as the primary symptom
Who cannot join
- Adherence to special diets (low-fat, lactose-free, or gluten-free diets) within the past six months Food allergies such as soy, nuts, or seafood allergies Insulin-dependent diabetes mellitus Celiac disease Inflammatory bowel disease History of major gastrointestinal surgery, including colonic surgery or cholecystectomy Bloody diarrhea, hematochezia, or melena Recent antibiotic use Presence of alarming gastrointestinal symptoms Severe renal disease Severe hepatic disease Pregnancy Breastfeeding
Trial locations and contacts
1 site in 1 country.
About this study
Official title: A Pilot Quasi-experimental Study Evaluating a Standardized Boswellia Carterii Extract Combined With Structured Patient Education in IBS
Irritable bowel syndrome (IBS) is a common condition that affects the stomach and intestines. It can cause abdominal pain, bloating, diarrhea, constipation, and changes in bowel habits, which may reduce a person's quality of life. Many people with IBS do not achieve complete symptom relief with standard treatments.
The purpose of this study is to evaluate whether a standardized Boswellia extract, combined with structured patient education, can help improve IBS symptoms and quality of life. Boswellia is a herbal extract that may help reduce inflammation and digestive discomfort.
Read more
In this study, 60 adults aged 18-39 years with moderate IBS were enrolled at Mansoura University Hospitals, Egypt. Participants received 500 mg of standardized Boswellia extract twice daily for 30 days and attended educational sessions about IBS self-management, including symptom control and healthy lifestyle practices.
Researchers evaluated abdominal pain, bloating, bowel habits, other gastrointestinal symptoms, and quality of life at the start of the study, after one week, and after one month to determine whether the intervention improved IBS symptoms and daily functioning.
Read the detailed description
Irritable bowel syndrome (IBS) is a common and often debilitating gastrointestinal disorder characterized by recurrent abdominal pain, bloating, and altered bowel habits without identifiable structural pathology. Diagnosis relies primarily on symptom-based criteria and the exclusion of other conditions, with IBS defined as abdominal discomfort or pain associated with changes in bowel habits for at least three months. IBS is among the most frequently encountered gastrointestinal conditions in both primary and secondary care. Advances in research and updates from the British Society of Gastroenterology have re-framed IBS as a disorder of gut-brain interaction (DGBI) rather than a purely functional disorder, with over 40% of individuals worldwide estimated to meet diagnostic criteria for at least one DGBI during their lifetime. [1,2,4].Study Design and Setting
This quasi-experimental study was conducted to assess the effects of standardized Boswellia Cartteri extract on abdominal bloating, abdominal pain, and quality of life in patients with irritable bowel syndrome (IBS). The study took place at the outpatient clinics of Mansoura University Hospitals.
Participant and Sampling
Inclusion criteria Adult patients with moderate IBS were recruited through convenience sampling. Eligible participants were aged 18-39 years, literate, and reported bloating as their primary symptom. IBS diagnosis was confirmed according to Rome III and IV criteria, which require recurrent abdominal pain at least once weekly over the preceding three months, accompanied by changes in stool frequency, form, or defecation.
Exclusion criteria included adherence to special diets (low-fat, lactose-free, gluten-free) within the past six months, food allergies (e.g., soy, nuts, seafood), insulin-dependent diabetes, celiac disease, inflammatory bowel disease, prior major gastrointestinal surgery(colonic surgery, or cholecystectomy), Bloody diarrhea, hematochezia or melanic stools, recent antibiotic use, alarming gastrointestinal symptoms, severe renal or hepatic disease, pregnancy, and breastfeeding.
Sample Size A minimum of 60 participants was determined using G*Power software, accounting for a 30% dropout rate. The calculation assumed a significance level of 0.05, 95% statistical power, and a large effect size (0.8), based on prior studies examining the effects of Boswellia Cartter on abdominal bloating.( Kazemian, Yuan, Cochran, \& Khoshnevis, 2017).
Data Collection Instruments
Four validated instruments were employed for data collection:
- Sociodemographic and Lifestyle Questionnaire A structured, self-administered questionnaire was used to collect information on participants' age, gender, education, marital status, occupation, smoking habits, income, sleep adequacy, and other relevant lifestyle factors.
- Gastrointestinal Symptom Assessment (Rome III \& IV) Gastrointestinal symptoms were evaluated using an adapted Rome-based questionnaire, which assessed abdominal pain, bloating, stool frequency and form, bowel habit sub-type, and symptom relief following defecation. Responses were recorded as categorical or dichotomous variables. ( Lacy and Patel 2017) and Goodoory, V. C., Houghton, L. A., Yiannakou, Y., Black, C. J., \& Ford, A. C. 2022).
Tool III: Abdominal bloatingand pain score questionnaire:
The researcher used this tool to assess patients' experience of bloating/uncomfortably full on a scale of none (no symptom), mild (does not interfere with activities), moderate (somewhat interferes with activities), and severe (renders usual activities impossible). The researcher adapted the tool from Lacy, Cangemi, Wise and Crowell (2021) The frequency of bloating was assessed by recording the number of days participants experienced bloating during the previous seven days, coded as an integer variable ranging from 0 to 7. Pain intensity was measured using a numerical rating scale (0-10), and additional details such as pain location, quality, and pattern were documented. It was measured using a numerical rating scale ranging from 0 (no pain) to 10 (worst possible pain) (Mujagic, et al.,2015; Karcioglu, Topacoglu, Dikme, \& Dikme, 2018).
Tool V: quality of life assessment structured questionnaire The researcher used this tool to assess work absences, social life, sleep, and leisure activities, physical, psychological, and financial aspects. The researcher adapted the tool
Irritable bowel syndrome also imposes a substantial economic burden on healthcare systems worldwide, with significant direct and indirect costs reported across the United States, Europe, and Asia [1].
The pathophysiology of IBS is multi factorial, involving interactions among dietary factors, gut microbiota alterations, visceral hypersensitivity, immune dysregulation, and genetic predisposition. Contributions of these mechanisms may vary across populations due to cultural, geographic, and environmental differences. While IBS was historically considered functional, emerging evidence supports a biopsychosocial model emphasizing altered brain-gut communication, as reflected in the Rome IV diagnostic criteria. Recent studies highlight the role of low-grade inflammation and immune dysregulation in IBS pathogenesis. Bioactive triterpenoids from Boswellia carterii (frankincense) have been shown to regulate immune cell activity and inflammatory signaling pathways, including inhibition of 5-lipoxygenase and leukotriene synthesis, providing a biological rationale for their potential therapeutic effects in IBS. [5,6,7].
In addition, Boswellia-derived compounds have been demonstrated to inhibit leukotriene synthesis through suppression of 5-lipoxygenase activity, a key inflammatory pathway implicated in immune activation and tissue inflammation. Natural leukotriene inhibitors isolated from Boswellia have shown potent anti-inflammatory effects, supporting their relevance in inflammatory disorders. Given the emerging role of leukotriene-mediated low-grade inflammation in IBS pathophysiology, this mechanism offers further biological plausibility for symptom improvement associated with Boswellia supplementation [8].
Bloating, affecting over 90% of IBS patients, is among the most distressing symptoms and significantly reduces quality of life, contributing to psychological distress, impaired productivity, and social embarrassment. Overall, IBS negatively impacts daily functioning, occupational performance, and social participation. Despite its prevalence, challenges in diagnosis and treatment often delay effective management, and conventional pharmacological therapies primarily provide symptom relief, sometimes with limited efficacy or adverse effects. Consequently, many patients turn to complementary approaches, including dietary modifications and herbal therapies. Multidisciplinary management, incorporating physicians, nurses, dietitians, and psychologists, alongside patient education and self-management interventions, has been shown to improve symptom control and quality of life. [5,9,10,11].
Given the chronic nature of IBS, the limitations of current treatments, and growing interest in complementary therapies, investigating the effects of standardized Boswellia extract offers a promising avenue for adjunctive management of IBS.
- Conditions
- Irritable Bowel Syndrome
- Being tested
- Boswellia carterii Extract, Educationntal program for IBS patie
- Keywords
- Boswellia extract Complementary therapy Gut-brain axis Quality of life
- Medical subject headings
- Irritable Bowel Syndrome
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Boswellia carterii ExtractDrug
A soft gelatin capsule containing 500 mg of standardized Boswellia extract (containing more than 65% Boswellia acids) was administered orally twice daily with meals for a duration of 30 days. The researcher met with the participants five times per week at the outpatient clinics of Mansoura University Hospitals. During these meetings, participants were instructed on the proper administration of the capsules and were informed about potential side effects, including headache, diarrhea, renal complications, weight gain, osteoporosis, increased risk of infection, and high cost. In addition, the researcher conducted weekly follow-up phone calls, particularly during the first week of treatment, to assess the occurrence of any allergic reactions or adverse effects related to the Boswellia capsules. These follow-ups also aim to monitor adherence to the intervention, identify any missed doses, and obtain feedback regarding participants perceived improvement.
Educationntal program for IBS patieOther
The researchers analyzed the findings from the assessment phase to identify gaps in knowledge and areas requiring improvement. Based on this analysis, the program's objectives and content were designed to address the specific educational needs of the IBS patients. All potential participants underwent an initial assessment to ensure that they met the inclusion criteria and did not meet any of the exclusion criteria. Demographic characteristics and relevant health-related data were collected from participants on the first day of the study using data collection tools as mentioned above. Educational sessions were provided to participants regarding irritable bowel syndrome (IBS) and the importance of Boswellia in the management of IBS
| Study group | Role | What they receive |
|---|---|---|
| Participants received 500 mg standardized Boswellia extract (≥65% boswellic acids) twice daily | Experimental | Phytochemical standardization of the Boswellia carterii oleogum resin extract was conducted at the FAB-Lab (Faculty of Pharmacy, Mansoura University) to ensure batch-to-batch consistency and defined bioactive content. The extract was standardized to contain ≥65% total boswellic acids, based on previously established analytical and isolation methodologies developed in our laboratory. These procedures include chromatographic separation and characterization of immunomodulatory triterpenoids(7), as well as validation of leukotriene-inhibitory activity and bioactive compound profiling, as described in earlier pharmacological and clinical investigations of Boswellia preparations(8). The standardization approach has been consistently applied in prior experimental and clinical studies evaluating anti-inflammatory, immunomodulatory, antiviral, and osteoarthritis-related therapeutic effects of Boswellia-derived compounds, thereby ensuring reproducibility, phytochemical integrity, and biological Receives: Drug: Boswellia carterii Extract; Other: Educationntal program for IBS patie |
What is being measured
The primary outcome is the main question the study is designed to answer.
This study aims to assess effects of standardized Boswellia extract on irritable bowel syndrome patients
H1: Patients with irritable bowel syndrome (IBS) who take standardized boswellia extract will experience a reduction in abdominal bloating.
H1: Patients with IBS who take standardized boswellia extract will experience a reduction in abdominal pain.
H1: Patients with IBS who take standardized boswellia extract will improve their quality of life. Abdominal pain was assessed using a structured questionnaire. Pain location was coded as a categorical variable (1-4), pain quality as a categorical variable (1-4), and pain pattern as a categorical variable (1-2). Pain triggers were recorded as an open numeric variable. Pain intensity was measured using a numerical rating scale ranging from 0 (no pain) to 10 (worst possible pain. Pain intensity was measured using a numerical rating scale (0-10), and additional details such as pain location, quality, and pattern were documented. quality of life assessment structured questionnaire
The researcher used this tool to assess work absenteeism,
Measured: The study hypotheses was conducted at three time points: before the initiation of the intervention (baseline), one week after the intervention, and one month following the intervention.
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted8 May 2026
- Study start1 Jan 2025
- Primary completion30 Dec 2025
- Study completion30 Jan 2026
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Irritable Bowel SyndromeStudies of the same condition, open and under way.
- More trials run by Mansoura UniversityThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 2/3
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Model description
- In this quasi-experimental study, 60 adults (18-39 years) with moderate IBS were enrolled at Mansoura University Hospitals, Egypt. Participants received 500 mg standardized Boswellia extract (≥65% boswellic acids) twice daily for 30 days.In addition, Boswellia-derived compounds have been demonstrated to inhibit leukotriene synthesis through suppression of 5-lipoxygenase activity, a key inflammatory pathway implicated in immune activation and tissue inflammation. Natural leukotriene inhibitors isolated from Boswellia have shown potent anti-inflammatory effects, supporting their relevance in inflammatory disorders. Given the emerging role of leukotriene-mediated low-grade inflammation in IBS pathophysiology, this mechanism offers further biological plausibility for symptom improvement associated with Boswellia supplementation
- Masking
- None (open label)
- Enrolment
- 60 participants (actual)
Sponsor and investigators
- Lead sponsor
- Mansoura University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07576634
- Sponsor's protocol ID
- Boswellia on IBS patients
- Acronym
- BC-IBS
- Status last verified
- Apr 2026
- First submitted
- 3 Apr 2026
- Last updated
- 8 May 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 8 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Pilot Quasi-experimental Study Evaluating a Standardized Boswellia Carterii Extract Combined With Structured Patient Education in IBS
- ClinicalTrials.gov ID
- NCT07576634
- Acronym / sponsor ID
- BC-IBS / Boswellia on IBS patients
- Conditions
- Irritable Bowel Syndrome
- Keywords
- Boswellia extract Complementary therapy Gut-brain axis Quality of life
- Phase
- Phase 2/3
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 60 participants (actual)
- Lead sponsor
- Mansoura UniversityUniversity, hospital or other
- Study start
- 1 Jan 2025 (actual)
- Primary completion
- 30 Dec 2025 (actual)
- Study completion
- 30 Jan 2026 (actual)
- First posted
- 8 May 2026 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Irritable bowel syndrome (IBS) is a common condition that affects the stomach and intestines. It can cause abdominal pain, bloating, diarrhea, constipation, and changes in bowel habits, which may reduce a person's quality of life. Many people with IBS do not achieve complete symptom relief with standard treatments.
The purpose of this study is to evaluate whether a standardized Boswellia extract, combined with structured patient education, can help improve IBS symptoms and quality of life. Boswellia is a herbal extract that may help reduce inflammation and digestive discomfort.
In this study, 60 adults aged 18-39 years with moderate IBS were enrolled at Mansoura University Hospitals, Egypt. Participants received 500 mg of standardized Boswellia extract twice daily for 30 days and attended educational sessions about IBS self-management, including symptom control and healthy lifestyle practices.
Researchers evaluated abdominal pain, bloating, bowel habits, other gastrointestinal symptoms, and quality of life at the start of the study, after one week, and after one month to determine whether the intervention improved IBS symptoms and daily functioning.
Detailed description
Irritable bowel syndrome (IBS) is a common and often debilitating gastrointestinal disorder characterized by recurrent abdominal pain, bloating, and altered bowel habits without identifiable structural pathology. Diagnosis relies primarily on symptom-based criteria and the exclusion of other conditions, with IBS defined as abdominal discomfort or pain associated with changes in bowel habits for at least three months. IBS is among the most frequently encountered gastrointestinal conditions in both primary and secondary care. Advances in research and updates from the British Society of Gastroenterology have re-framed IBS as a disorder of gut-brain interaction (DGBI) rather than a purely functional disorder, with over 40% of individuals worldwide estimated to meet diagnostic criteria for at least one DGBI during their lifetime. [1,2,4].Study Design and Setting
This quasi-experimental study was conducted to assess the effects of standardized Boswellia Cartteri extract on abdominal bloating, abdominal pain, and quality of life in patients with irritable bowel syndrome (IBS). The study took place at the outpatient clinics of Mansoura University Hospitals.
Participant and Sampling
Inclusion criteria Adult patients with moderate IBS were recruited through convenience sampling. Eligible participants were aged 18-39 years, literate, and reported bloating as their primary symptom. IBS diagnosis was confirmed according to Rome III and IV criteria, which require recurrent abdominal pain at least once weekly over the preceding three months, accompanied by changes in stool frequency, form, or defecation.
Exclusion criteria included adherence to special diets (low-fat, lactose-free, gluten-free) within the past six months, food allergies (e.g., soy, nuts, seafood), insulin-dependent diabetes, celiac disease, inflammatory bowel disease, prior major gastrointestinal surgery(colonic surgery, or cholecystectomy), Bloody diarrhea, hematochezia or melanic stools, recent antibiotic use, alarming gastrointestinal symptoms, severe renal or hepatic disease, pregnancy, and breastfeeding.
Sample Size A minimum of 60 participants was determined using G*Power software, accounting for a 30% dropout rate. The calculation assumed a significance level of 0.05, 95% statistical power, and a large effect size (0.8), based on prior studies examining the effects of Boswellia Cartter on abdominal bloating.( Kazemian, Yuan, Cochran, \& Khoshnevis, 2017).
Data Collection Instruments
Four validated instruments were employed for data collection:
- Sociodemographic and Lifestyle Questionnaire A structured, self-administered questionnaire was used to collect information on participants' age, gender, education, marital status, occupation, smoking habits, income, sleep adequacy, and other relevant lifestyle factors.
- Gastrointestinal Symptom Assessment (Rome III \& IV) Gastrointestinal symptoms were evaluated using an adapted Rome-based questionnaire, which assessed abdominal pain, bloating, stool frequency and form, bowel habit sub-type, and symptom relief following defecation. Responses were recorded as categorical or dichotomous variables. ( Lacy and Patel 2017) and Goodoory, V. C., Houghton, L. A., Yiannakou, Y., Black, C. J., \& Ford, A. C. 2022).
Tool III: Abdominal bloatingand pain score questionnaire:
The researcher used this tool to assess patients' experience of bloating/uncomfortably full on a scale of none (no symptom), mild (does not interfere with activities), moderate (somewhat interferes with activities), and severe (renders usual activities impossible). The researcher adapted the tool from Lacy, Cangemi, Wise and Crowell (2021) The frequency of bloating was assessed by recording the number of days participants experienced bloating during the previous seven days, coded as an integer variable ranging from 0 to 7. Pain intensity was measured using a numerical rating scale (0-10), and additional details such as pain location, quality, and pattern were documented. It was measured using a numerical rating scale ranging from 0 (no pain) to 10 (worst possible pain) (Mujagic, et al.,2015; Karcioglu, Topacoglu, Dikme, \& Dikme, 2018).
Tool V: quality of life assessment structured questionnaire The researcher used this tool to assess work absences, social life, sleep, and leisure activities, physical, psychological, and financial aspects. The researcher adapted the tool
Irritable bowel syndrome also imposes a substantial economic burden on healthcare systems worldwide, with significant direct and indirect costs reported across the United States, Europe, and Asia [1].
The pathophysiology of IBS is multi factorial, involving interactions among dietary factors, gut microbiota alterations, visceral hypersensitivity, immune dysregulation, and genetic predisposition. Contributions of these mechanisms may vary across populations due to cultural, geographic, and environmental differences. While IBS was historically considered functional, emerging evidence supports a biopsychosocial model emphasizing altered brain-gut communication, as reflected in the Rome IV diagnostic criteria. Recent studies highlight the role of low-grade inflammation and immune dysregulation in IBS pathogenesis. Bioactive triterpenoids from Boswellia carterii (frankincense) have been shown to regulate immune cell activity and inflammatory signaling pathways, including inhibition of 5-lipoxygenase and leukotriene synthesis, providing a biological rationale for their potential therapeutic effects in IBS. [5,6,7].
In addition, Boswellia-derived compounds have been demonstrated to inhibit leukotriene synthesis through suppression of 5-lipoxygenase activity, a key inflammatory pathway implicated in immune activation and tissue inflammation. Natural leukotriene inhibitors isolated from Boswellia have shown potent anti-inflammatory effects, supporting their relevance in inflammatory disorders. Given the emerging role of leukotriene-mediated low-grade inflammation in IBS pathophysiology, this mechanism offers further biological plausibility for symptom improvement associated with Boswellia supplementation [8].
Bloating, affecting over 90% of IBS patients, is among the most distressing symptoms and significantly reduces quality of life, contributing to psychological distress, impaired productivity, and social embarrassment. Overall, IBS negatively impacts daily functioning, occupational performance, and social participation. Despite its prevalence, challenges in diagnosis and treatment often delay effective management, and conventional pharmacological therapies primarily provide symptom relief, sometimes with limited efficacy or adverse effects. Consequently, many patients turn to complementary approaches, including dietary modifications and herbal therapies. Multidisciplinary management, incorporating physicians, nurses, dietitians, and psychologists, alongside patient education and self-management interventions, has been shown to improve symptom control and quality of life. [5,9,10,11].
Given the chronic nature of IBS, the limitations of current treatments, and growing interest in complementary therapies, investigating the effects of standardized Boswellia extract offers a promising avenue for adjunctive management of IBS.
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- In this quasi-experimental study, 60 adults (18-39 years) with moderate IBS were enrolled at Mansoura University Hospitals, Egypt. Participants received 500 mg standardized Boswellia extract (≥65% boswellic acids) twice daily for 30 days.In addition, Boswellia-derived compounds have been demonstrated to inhibit leukotriene synthesis through suppression of 5-lipoxygenase activity, a key inflammatory pathway implicated in immune activation and tissue inflammation. Natural leukotriene inhibitors isolated from Boswellia have shown potent anti-inflammatory effects, supporting their relevance in inflammatory disorders. Given the emerging role of leukotriene-mediated low-grade inflammation in IBS pathophysiology, this mechanism offers further biological plausibility for symptom improvement associated with Boswellia supplementation
| Arm | Type | Receives |
|---|---|---|
| Participants received 500 mg standardized Boswellia extract (≥65% boswellic acids) twice daily | Experimental | Drug: Boswellia carterii Extract, Other: Educationntal program for IBS patiePhytochemical standardization of the Boswellia carterii oleogum resin extract was conducted at the FAB-Lab (Faculty of Pharmacy, Mansoura University) to ensure batch-to-batch consistency and defined bioactive content. The extract was standardized to contain ≥65% total boswellic acids, based on previously established analytical and isolation methodologies developed in our laboratory. These procedures include chromatographic separation and characterization of immunomodulatory triterpenoids(7), as well as validation of leukotriene-inhibitory activity and bioactive compound profiling, as described in earlier pharmacological and clinical investigations of Boswellia preparations(8). The standardization approach has been consistently applied in prior experimental and clinical studies evaluating anti-inflammatory, immunomodulatory, antiviral, and osteoarthritis-related therapeutic effects of Boswellia-derived compounds, thereby ensuring reproducibility, phytochemical integrity, and biological |
Who may qualify
- Ages
- 18 to 65 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (1 listed)
- Adults diagnosed with irritable bowel syndrome (IBS) according to Rome III and Rome IV criteria Recurrent abdominal pain occurring at least once weekly during the preceding three months Presence of changes in stool frequency, stool form, or defecation associated with abdominal pain Participants reporting bloating as the primary symptom
Key exclusion criteria (1 listed)
- Adherence to special diets (low-fat, lactose-free, or gluten-free diets) within the past six months Food allergies such as soy, nuts, or seafood allergies Insulin-dependent diabetes mellitus Celiac disease Inflammatory bowel disease History of major gastrointestinal surgery, including colonic surgery or cholecystectomy Bloody diarrhea, hematochezia, or melena Recent antibiotic use Presence of alarming gastrointestinal symptoms Severe renal disease Severe hepatic disease Pregnancy Breastfeeding
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Boswellia carterii ExtractA soft gelatin capsule containing 500 mg of standardized Boswellia extract (containing more than 65% Boswellia acids) was administered orally twice daily with meals for a duration of 30 days. The researcher met with the participants five times per week at the outpatient clinics of Mansoura University Hospitals. During these meetings, participants were instructed on the proper administration of the capsules and were informed about potential side effects, including headache, diarrhea, renal complications, weight gain, osteoporosis, increased risk of infection, and high cost. In addition, the researcher conducted weekly follow-up phone calls, particularly during the first week of treatment, to assess the occurrence of any allergic reactions or adverse effects related to the Boswellia capsules. These follow-ups also aim to monitor adherence to the intervention, identify any missed doses, and obtain feedback regarding participants perceived improvement. | Drug | Participants received 500 mg standardized Boswellia extract (≥65% boswellic acids) twice daily |
| Educationntal program for IBS patieThe researchers analyzed the findings from the assessment phase to identify gaps in knowledge and areas requiring improvement. Based on this analysis, the program's objectives and content were designed to address the specific educational needs of the IBS patients. All potential participants underwent an initial assessment to ensure that they met the inclusion criteria and did not meet any of the exclusion criteria. Demographic characteristics and relevant health-related data were collected from participants on the first day of the study using data collection tools as mentioned above. Educational sessions were provided to participants regarding irritable bowel syndrome (IBS) and the importance of Boswellia in the management of IBS | Other | Participants received 500 mg standardized Boswellia extract (≥65% boswellic acids) twice daily |
Primary outcome
This study aims to assess effects of standardized Boswellia extract on irritable bowel syndrome patients
Time frame: The study hypotheses was conducted at three time points: before the initiation of the intervention (baseline), one week after the intervention, and one month following the intervention.
H1: Patients with irritable bowel syndrome (IBS) who take standardized boswellia extract will experience a reduction in abdominal bloating. H1: Patients with IBS who take standardized boswellia extract will experience a reduction in abdominal pain. H1: Patients with IBS who take standardized boswellia extract will improve their quality of life. Abdominal pain was assessed using a structured questionnaire. Pain location was coded as a categorical variable (1-4), pain quality as a categorical variable (1-4), and pain pattern as a categorical variable (1-2). Pain triggers were recorded as an open numeric variable. Pain intensity was measured using a numerical rating scale ranging from 0 (no pain) to 10 (worst possible pain. Pain intensity was measured using a numerical rating scale (0-10), and additional details such as pain location, quality, and pattern were documented. quality of life assessment structured questionnaire The researcher used this tool to assess work absenteeism,
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 8 May 2026.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 2/3 study testing Boswellia carterii Extract and Educationntal program for IBS patie in people with Irritable Bowel Syndrome, run by Mansoura University at 1 site in Egypt.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 1 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 8 May 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this combined phase mean?
Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
This study aims to assess effects of standardized Boswellia extract on irritable bowel syndrome patients (time frame: The study hypotheses was conducted at three time points: before the initiation of the intervention (baseline), one week after the intervention, and one month following the intervention.). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 May 2026.