Chronic CholestasisNCT07569003
Prealbumin and IGF-1 Levels in Pediatric Chronic Cholestasis With Severe Malnutrition After Nutrition Therapy
A study testing Nutrition Therapy in people with Chronic Cholestasis and Severe Malnutrition, run by Universitas Indonesia at 1 site in Indonesia.
Trial summary
The goal of this clinical trial is to learn if a high-energy liquid diet improves the nutritional status of children with chronic cholestasis (a liver condition that blocks bile flow). Researchers want to see if this diet helps children who are malnourished. Read more about this study
- Who is it for?
- Ages Up to 5 years
- Conditions the study is for
- Chronic Cholestasis, Severe Malnutrition, Pediatric Cholestasis
- What is being tested?
- Nutrition Therapy
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 15 participants
- Where
- 1 siteIndonesia
- Study dates
- 6 Apr 2026to Jul 2026
- Phase
- Interventional
- Are there results?
- Not yet: the study is under way
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 Up to 5 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Children under 5 years old
- Diagnosed with chronic cholestasis and severe malnutrition
- Parental/guardian informed consent
- Willingness to use a nasogastric tube (NGT) if indicated
- Covered by national health insurance or other insurance
Who cannot join
- Comorbidities (heart failure, chronic kidney disease, HIV)
- Severe acute infections (acute gastroenteritis, dengue fever, pneumonia)
- Post-liver transplant
- Post-Kasai portoenterostomy (jaundice-free)
- Currently exclusively breastfeeding
- Use of steroids or NSAIDs within two weeks prior to the study.
- Receiving a transfusion of whole blood, fresh frozen plasma, or platelets within one week prior to the study
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Indonesia1 site, 1 recruiting
- Recruiting
Faculty of Medicine, University of Indonesia, Jakarta, DKI Jakarta 10430
Jakarta Pusat, DKI Jakarta, 10430
Tri Faranita, dr., Sp.A, +628126016641, faranita.md@gmail.com
Klara Yuliarti, Dr., dr., Sp.A(K), klarayuliarti@yahoo.com
About this study
Official title: Preliminary Study: Effect of Nutrition Therapy on Prealbumin and IGF-1 Level in Severe Malnutrition Under Five Years Old With Chronic Cholestasis
The goal of this clinical trial is to learn if a high-energy liquid diet improves the nutritional status of children with chronic cholestasis (a liver condition that blocks bile flow). Researchers want to see if this diet helps children who are malnourished.
The main questions the study aims to answer are:
Read more
- Does the liquid diet raise the level of prealbumin (a marker of nutrition) in the blood?
- Does the liquid diet raise the level of Insulin-like Growth Factor-1 (IGF-1) (a hormone that helps growth) in the blood?
Participants will:
- Consume a high-energy liquid diet for 14 days.
- Give blood samples at the start and at the end of the 2-week study.
- Keep a daily record of what they eat and drink in a food diary. Researchers will compare the blood test results from the start and the end of the study to see if the liquid diet works to improve the children's prealbumin and IGF-1 levels. This study is important to help children with liver problems grow better and stay healthy.
Read the detailed description
The study evaluates the effect of nutritional therapy on prealbumin levels and insulin-like growth factor-1 (IGF-1) levels in malnourished children with chronic cholestasis aged 3-59 months (primary outcome) and diet tolerance, nutritional status, and medical condition (secondary outcomes).
Prealbumin and IGF-1 levels are measured as primary outcomes at baseline (day 0) and at day 15. Diet tolerance is assessed using the Bristol Stool Chart, a daily vomiting record throughout the 14-day intervention period, and allergic reactions. The frequency of defecation and consistency of each stool are documented. Allergic reactions are also monitored during the intervention period, including symptoms such as fever, erythematous rash, pruritus, and respiratory symptoms such as shortness of breath. The onset, duration, and severity of these symptoms are recorded.
Vomiting is evaluated as the number of episodes per day over the 14-day intervention period, and the volume of each episode is recorded. Only vomiting attributable to diet intolerance is included in the analysis, while episodes related to other causes, such as coughing or crying, are excluded.
Anthropometric parameters, including weight, height, mid-upper arm circumference, and other relevant measurements, are assessed on day 0, day 8, and day 15 to monitor changes in nutritional status.
Medical conditions during the study period are closely monitored, including underlying diseases, comorbidities, and intercurrent illnesses (e.g., respiratory or gastrointestinal infections). Clinical changes, hospitalizations, medication use, and any complications occurring during the intervention are recorded to evaluate their potential impact on nutritional status and study outcomes.
Nutritional therapy is administered as a liquid diet providing 130% of the recommended daily allowance (RDA), with macronutrient and micronutrient composition adjusted according to the 2019 ESPGHAN and 2021 Tessitore guidelines, over a 14-day intervention period. To ensure accurate nutritional intake, feeding is administered via a nasogastric tube, with gradual advancement of caloric intake until reaching 130% of RDA by day 4. Feeding is performed by parents or caregivers who are trained in proper administration techniques, feeding schedules, and hygiene practices. Monitoring of dietary adherence is conducted by daily food recall, instant messaging, and video call supervision during feeding sessions.
Protocol for nutritional therapy advancement is as follows:
- Calorie requirement is calculated by multiplying ideal body weight with daily energy requirement (recommended dietary allowance, RDA).
- Ideal body weight is defined as the median weight for actual height based on WHO growth charts (weight-for-height/length).
- Height age is defined as the median age corresponding to the patient's actual height based on WHO growth charts (height/length-for-age).
- The target energy intake is set at 130% of RDA according to height age, in line with ESPGHAN 2019 and Tessitore 2021 recommendations.
- On the first day: patients are provided with 44 to 140 more calories than their usual daily intake, based on the results of a food recall analysis. Nutritional therapy is administered as a liquid diet via a nasogastric tube, divided into 8 feeding sessions per day (every 3 hours).
- On the second day to fourth day: caloric intake is gradually increased until reaching 130% of RDA on the fourth day. The feeding regimen (volume and frequency) is adjusted according to patient tolerance.
- From fourth day to fourteenth day: the patient is maintained on full nutritional therapy at 130% of RDA. Monitoring of intake is conducted through daily food recall and communication via instant messaging/video calls.
Adjustments to feeding (volume, frequency, or rate) are made based on diet tolerance. If gastrointestinal intolerance or metabolic complications occur, nutritional therapy is modified according to clinical guidelines.
- Being tested
- Nutrition Therapy
- Keywords
- Chronic Cholestasis, Severe malnutrition, Pediatric cholestasis, IGF-1, Prealbumin, Nutrition therapy
- Medical subject headings
- Malnutrition
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Nutrition TherapyOther
The nutritional therapy provided consists of a liquid formula with BPOM approval number MD 250976001600096 for subjects under 1 year of age, and BPOM approval number ML 562409102696 for subjects over 1 year of age. Patients are also given micronutrients in the form of vitamins A, D, E, and K, as well as vitamin B1, folic acid, and zinc as needed.
| Study group | Role | What they receive |
|---|---|---|
| Nutrition Therapy Group | Experimental | Nutrition therapy Receives: Other: Nutrition Therapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
Prealbumin and IGF-1 levels
The difference in prealbumin and IGF-1 levels before and after 14 days of nutritional therapy
Measured: 15 days
Secondary outcomes (8)
Gastrointestinal tolerance for bowel movement
Frequency of bowel movement per day and description of stool consistency (Bristol stool chart)
Measured: 14 days
Mid upper arm circumference changes
Mid upper arm circumference changes is assessed using upper arm circumference measurements on the day of baseline and on the fifteenth day (after 14 days of nutritional intervention)
Measured: 15 days
Height gain
Height gain is a change in height measured in centimetres with 1 decimal. The height gain is defined as the height on day 15 minus the height on day 0. Height on day 0 and day 15 will also be plotted on the WHO Growth Chart height-for-age z-score, and the change of height-for-age z-score will also be measured.
Measured: 15 days
Other illness duration
Other illness duration refer to the duration of other illness (patient's illness unrelated to their primary illness) in days during the study.
Measured: 14 days
Gastrointestinal tolerance for vomit
Frequency of vomit per day and volume of vomit
Measured: 14 days
Prevalence of allergic reaction
Prevalence of subjects whom seems to have allergic reactions (rashes on skin) after receiving nutritional therapy
Measured: 14 days
Prevalence of vomiting
Prevalence of participants experiencing vomiting after receiving nutrition therapy
Measured: 14 days
Prevalence of diarrhea
Prevalence of participants experiencing diarrhea after receiving nutritional therapy
Measured: 14 days
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted6 May 2026
- Study start6 Apr 2026
- Primary completionJun 2026 (estimated)
- Study completionJul 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Chronic CholestasisStudies of the same condition, open and under way.
- More trials run by Universitas IndonesiaThe 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 N/A
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- Pre and post design
- Masking
- None (open label)
- Enrolment
- 15 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Universitas Indonesia
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, dr. Tri Faranita, MKed(Ped), SpA, Universitas Indonesia
- Investigators
- Tri Faranita, dr, Sp.A, Principal investigator, Department of Child Health, Faculty of Medicine, University of Indonesia - Cipto Mangunkusumo Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07569003
- Sponsor's protocol ID
- 25-12-1945
- Status last verified
- May 2026
- First submitted
- 14 Apr 2026
- Last updated
- 6 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 6 May 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Preliminary Study: Effect of Nutrition Therapy on Prealbumin and IGF-1 Level in Severe Malnutrition Under Five Years Old With Chronic Cholestasis
- ClinicalTrials.gov ID
- NCT07569003
- Acronym / sponsor ID
- 25-12-1945
- Keywords
- Chronic Cholestasis, Severe malnutrition, Pediatric cholestasis, IGF-1, Prealbumin, Nutrition therapy
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 15 participants (estimated)
- Lead sponsor
- Universitas IndonesiaUniversity, hospital or other
- Study start
- 6 Apr 2026 (actual)
- Primary completion
- Jun 2026 (estimated)
- Study completion
- Jul 2026 (estimated)
- First posted
- 6 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.
The goal of this clinical trial is to learn if a high-energy liquid diet improves the nutritional status of children with chronic cholestasis (a liver condition that blocks bile flow). Researchers want to see if this diet helps children who are malnourished.
The main questions the study aims to answer are:
- Does the liquid diet raise the level of prealbumin (a marker of nutrition) in the blood?
- Does the liquid diet raise the level of Insulin-like Growth Factor-1 (IGF-1) (a hormone that helps growth) in the blood?
Participants will:
- Consume a high-energy liquid diet for 14 days.
- Give blood samples at the start and at the end of the 2-week study.
- Keep a daily record of what they eat and drink in a food diary. Researchers will compare the blood test results from the start and the end of the study to see if the liquid diet works to improve the children's prealbumin and IGF-1 levels. This study is important to help children with liver problems grow better and stay healthy.
Detailed description
The study evaluates the effect of nutritional therapy on prealbumin levels and insulin-like growth factor-1 (IGF-1) levels in malnourished children with chronic cholestasis aged 3-59 months (primary outcome) and diet tolerance, nutritional status, and medical condition (secondary outcomes).
Prealbumin and IGF-1 levels are measured as primary outcomes at baseline (day 0) and at day 15. Diet tolerance is assessed using the Bristol Stool Chart, a daily vomiting record throughout the 14-day intervention period, and allergic reactions. The frequency of defecation and consistency of each stool are documented. Allergic reactions are also monitored during the intervention period, including symptoms such as fever, erythematous rash, pruritus, and respiratory symptoms such as shortness of breath. The onset, duration, and severity of these symptoms are recorded.
Vomiting is evaluated as the number of episodes per day over the 14-day intervention period, and the volume of each episode is recorded. Only vomiting attributable to diet intolerance is included in the analysis, while episodes related to other causes, such as coughing or crying, are excluded.
Anthropometric parameters, including weight, height, mid-upper arm circumference, and other relevant measurements, are assessed on day 0, day 8, and day 15 to monitor changes in nutritional status.
Medical conditions during the study period are closely monitored, including underlying diseases, comorbidities, and intercurrent illnesses (e.g., respiratory or gastrointestinal infections). Clinical changes, hospitalizations, medication use, and any complications occurring during the intervention are recorded to evaluate their potential impact on nutritional status and study outcomes.
Nutritional therapy is administered as a liquid diet providing 130% of the recommended daily allowance (RDA), with macronutrient and micronutrient composition adjusted according to the 2019 ESPGHAN and 2021 Tessitore guidelines, over a 14-day intervention period. To ensure accurate nutritional intake, feeding is administered via a nasogastric tube, with gradual advancement of caloric intake until reaching 130% of RDA by day 4. Feeding is performed by parents or caregivers who are trained in proper administration techniques, feeding schedules, and hygiene practices. Monitoring of dietary adherence is conducted by daily food recall, instant messaging, and video call supervision during feeding sessions.
Protocol for nutritional therapy advancement is as follows:
- Calorie requirement is calculated by multiplying ideal body weight with daily energy requirement (recommended dietary allowance, RDA).
- Ideal body weight is defined as the median weight for actual height based on WHO growth charts (weight-for-height/length).
- Height age is defined as the median age corresponding to the patient's actual height based on WHO growth charts (height/length-for-age).
- The target energy intake is set at 130% of RDA according to height age, in line with ESPGHAN 2019 and Tessitore 2021 recommendations.
- On the first day: patients are provided with 44 to 140 more calories than their usual daily intake, based on the results of a food recall analysis. Nutritional therapy is administered as a liquid diet via a nasogastric tube, divided into 8 feeding sessions per day (every 3 hours).
- On the second day to fourth day: caloric intake is gradually increased until reaching 130% of RDA on the fourth day. The feeding regimen (volume and frequency) is adjusted according to patient tolerance.
- From fourth day to fourteenth day: the patient is maintained on full nutritional therapy at 130% of RDA. Monitoring of intake is conducted through daily food recall and communication via instant messaging/video calls.
Adjustments to feeding (volume, frequency, or rate) are made based on diet tolerance. If gastrointestinal intolerance or metabolic complications occur, nutritional therapy is modified according to clinical guidelines.
Study design
- Primary purpose
- Treatment
- Allocation
- Not applicable
- Intervention model
- Single group
- Masking
- None (open label)
- Number of arms
- 1
- Model description
- Pre and post design
| Arm | Type | Receives |
|---|---|---|
| Nutrition Therapy Group | Experimental | Other: Nutrition TherapyNutrition therapy |
Who may qualify
- Ages
- Up to 5 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (5 listed)
- Children under 5 years old
- Diagnosed with chronic cholestasis and severe malnutrition
- Parental/guardian informed consent
- Willingness to use a nasogastric tube (NGT) if indicated
- Covered by national health insurance or other insurance
Key exclusion criteria (7 listed)
- Comorbidities (heart failure, chronic kidney disease, HIV)
- Severe acute infections (acute gastroenteritis, dengue fever, pneumonia)
- Post-liver transplant
- Post-Kasai portoenterostomy (jaundice-free)
- Currently exclusively 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 |
|---|---|---|
| Nutrition TherapyThe nutritional therapy provided consists of a liquid formula with BPOM approval number MD 250976001600096 for subjects under 1 year of age, and BPOM approval number ML 562409102696 for subjects over 1 year of age. Patients are also given micronutrients in the form of vitamins A, D, E, and K, as well as vitamin B1, folic acid, and zinc as needed. | Other | Nutrition Therapy Group |
Primary outcome
Prealbumin and IGF-1 levels
Time frame: 15 days
The difference in prealbumin and IGF-1 levels before and after 14 days of nutritional therapy
8 secondary outcomes
Gastrointestinal tolerance for bowel movement
Time frame: 14 days
Mid upper arm circumference changes
Time frame: 15 days
Height gain
Time frame: 15 days
Other illness duration
Time frame: 14 days
Gastrointestinal tolerance for vomit
Time frame: 14 days
Prevalence of allergic reaction
Time frame: 14 days
Prevalence of vomiting
Time frame: 14 days
Prevalence of diarrhea
Time frame: 14 days
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 6 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.
Tri Faranita, dr, Sp.A principal investigator
Department of Child Health, Faculty of Medicine, University of Indonesia - Cipto Mangunkusumo Hospital
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Nutrition Therapy in people with Chronic Cholestasis and Severe Malnutrition, run by Universitas Indonesia at 1 site in Indonesia.
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 5 inclusion and 7 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: looking for participants now, as of the sponsor's last update on 6 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 Indonesia. 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.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Tri Faranita, dr, Sp.A (+628126016641, tri.faranita@ui.ac.id), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Prealbumin and IGF-1 levels (time frame: 15 days). 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 6 May 2026.