Corrosive InjuryPhase 3NCT07229456
Evaluation of the Role of N Acetyl Cysteine and Vitamin D in Improving Outcomes After Corrosive Ingestion
A Phase 3 study testing N Acetyl Cysteine and Vitamin D (Cholecalciferol ) in people with Corrosive Injury, run by Ain Shams University at 1 site in Egypt.
Trial summary
The goal of this clinical trial is to learn if N acetyl cysteine and vitaminD work to improve outcomes after corrosive ingestion in children. The main questions it aims to answer are: Does N acetyl cysteine and vitamin D decrease incidence of strictures after corrosive ingestion in children. Read more about this study
- Who is it for?
- Ages Up to 18 years
- Conditions the study is for
- Corrosive Injury
- What is being tested?
- N Acetyl Cysteine and Vitamin D (Cholecalciferol )
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 80 participants
- Where
- 1 siteEgypt
- Study dates
- 1 Oct 2024to 1 Dec 2025
- Phase
- Phase 3
- 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 18 years
- All sexes
- No healthy volunteers
- Child, Adult
Who may be able to join
- The study included all patients aged from 0 to 18 years old, of both sex, admitted to the PCC-ASUH with confirmed history of corrosive ingestion and exhibiting moderate or severe symptoms (as determined by Poisoning Severity Score 2 or 3, respectively) and DROOL score (Drooling, Reluctance, Oropharynx, Others, and leukocytosis) ≤ 6
Who cannot join
- o Asymptomatic patients.
- Patients exposed to corrosives through routes other than ingestion (e.g., inhalation, dermal or eye contact).
- Patients with a delay time of more than 24 h.
- Patients who co-ingested other poisons.
- Patients presented with GIT perforation after corrosive ingestion.
- Patients who received treatment before admission.
Show all 10Show fewer
- Patients receiving chemotherapy or radiation.
- Patients with known blood disorders or malignancy.
- Patients with history of blood transfusion in the last 90 days.
- Patients with recent infections in the last 14 day
Trial locations and contacts
1 site in 1 country.
About this study
The goal of this clinical trial is to learn if N acetyl cysteine and vitaminD work to improve outcomes after corrosive ingestion in children.
The main questions it aims to answer are:
Read more
Does N acetyl cysteine and vitamin D decrease incidence of strictures after corrosive ingestion in children.
Researchers will compare the effect of N acetyl cysteine and vitamin D in decreasing complication , length of hospital stay and start of complete oral intake Eighty patients were randomly assigned into four groups (1 control and 3 intervention groups 20 patients each)
Group 1 (Control group):
- Patients allocated in this group received the standard treatment protocol only according to PCC-ASUH guidelines
Group 2 (NAC group):
- Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to NAC with loading dose of 150 mg/kg diluted in 200 ml dextrose 5% or saline over 1 hour, followed by a maintenance dose of 50 mg/kg diluted in 500 ml of dextrose 5% or saline over 4 hours then followed by 100 ml/kg diluted in 1000 ml of dextrose 5% or saline over 16 hours
Group 3 (Vitamin D group):
Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to vitamin D in a single intramuscular high-dose (300,000 IU) which was given to all patients regardless patient's age
Group 4 (NAC+Vitamin D group):
Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to both vitamin D and NAC, in the same doses as groups (2 and 3
Read the detailed description
The current study is a controlled randomized, single-blinded clinical trial, conducted on acutely poisoned patients with confirmed history of corrosive ingestion who were admitted to the Poison Control Center, Ain Shams University Hospitals (PCC-ASUH) The required sample size is 80 patients, 20 patients in each group according to the recommendation of statistics committee (Community Medicine, Environmental, and Occupational Medicine Department - Faculty of Medicine, Ain shams University)
Eighty patients were randomly assigned into four groups (1 control and 3 intervention groups 20 patients each)
Group 1 (Control group):
- Patients allocated in this group received the standard treatment protocol only according to PCC-ASUH guideline This included patient stabilization, maintaining patent airways, oxygen administration and ventilatory support when necessary.
In patients presenting with oral symptoms such as lip edema, excessive drooling (sialorrhea), or oral ulcers, the child was kept NPO to prevent further irritation. Topical treatments including antibiotics, anti-inflammatory agents, and antifungals were applied to manage local infection and inflammation.
Intravenous fluids were started to maintain hydration, with the volume calculated based on the Holliday-Segar method as follows: 100 mL/kg for the first 10 kg of body weight, 50 mL/kg for the next 10 kg, and 20 mL/kg for any weight above 20 kg. Fluid selection depended on the clinical condition where isotonic fluids such as 0.9% saline were often used initially, followed by hypotonic solutions containing dextrose and electrolytes for maintenance to prevent complications like hyponatremia or fluid overload Corticosteroids, especially dexamethasone, were administered when there was severe lip edema or suspected airway swelling to reduce inflammation and to prevent airway compromise. The typical dose used was 0.6 mg/kg, up to a maximum of 10 mg. However, steroids were avoided in children presenting with hematemesis or melena, due to the risk of worsening gastrointestinal bleeding.
In cases with GIT symptoms, supportive care was provided. If vomiting was present, ondansetron was administered at a dose of 4 mg every 8 hours until symptoms were controlled, and then on demand. To treat esophagitis and abdominal discomfort, proton pump inhibitors (PPIs) such as omeprazole were used to reduce acid secretion and promote healing of the mucosa. Omeprazole was given at 0.4-0.8 mg/kg, either every 12 or 24 hours, depending on symptom severity.
For children with signs of upper GI bleeding such as hematemesis or melena, urgent resuscitation was initiated. This included blood transfusion in cases of hemoglobin drop, fresh frozen plasma, IV PPI infusion, and hemostatic agents like tranexamic acid (Kapron), etamsylate (Dicynone), and vitamin K (Konakion). Diagnostic imaging such as chest X-ray, erect and supine abdominal X-rays, and abdominal ultrasound were performed to assess complications like perforation or effusion.
In children with respiratory symptoms, especially those with stridor or laryngeal edema, adrenaline was administered to reduce airway swelling. If chemical pneumonitis was suspected, inhaled bronchodilators (e.g., salbutamol every 4-6 hours), mucolytics like N-acetyl cysteine (NAC) or hypertonic saline every 6 hours, and antibiotics (based on culture and sensitivity) were given. Additionally, IV paracetamol at 10-15 mg/kg every 6 hours was used for fever, pain, and inflammation.
For patients who developed dysphagia and could not tolerate oral or enteral feeding for more than 3-5 days, total parenteral nutrition (TPN) was initiated to prevent malnutrition and support tissue healing. TPN was carefully tailored to the child's age, weight, and clinical status. Fluid needs were typically 100-150 mL/kg/day. Glucose, the main energy source, was started at 6-8 mg/kg/min in neonates (up to 12-14 mg/kg/min as tolerated) and 5-10 mg/kg/min in older children. Amino acids, essential for growth and repair, were given at 2-3 g/kg/day in neonates and 1-2 g/kg/day in older children. Lipids were started early at 1-2 g/kg/day, increasing to 3 g/kg/day if needed, particularly in neonates.
Electrolyte supplementation was guided by lab values: sodium (2-5 mEq/kg/day), potassium (1-3 mEq/kg/day), calcium (50-100 mg/kg/day of elemental calcium), magnesium (0.25-0.5 mEq/kg/day), and phosphate (1-2 mmol/kg/day). Micronutrients were also essential - daily multivitamins were given (e.g.,1 mL/day for infants, 2-5 mL/day for older children), along with trace elements such as zinc (100-400 mcg/kg/day), copper (20 mcg/kg/day), manganese (1 mcg/kg/day), selenium (2 mcg/kg/day), and chromium (0.14-0.2 mcg/kg /day).
Group 2 (NAC group):
- Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to NAC with loading dose of 150 mg/kg diluted in 200 ml dextrose 5% or saline over 1 hour, followed by a maintenance dose of 50 mg/kg diluted in 500 ml of dextrose 5% or saline over 4 hours then followed by 100 ml/kg diluted in 1000 ml of dextrose 5% or saline over 16 hours
Preparation and administration of NAC were adjusted according to the age of the patient. In those>12 years old, total volume (NAC and IV fluid) for the bolus, 4-hour infusion, and 16 hours infusion was 200 ml, 500 ml, and 1 liter, respectively. In children <12 years but over 20 kg, volumes were 100 ml, 250 ml, and 500 ml, respectively. In those under 20 kg, volumes were 3 ml/kg, 7 ml/kg, and 14 ml/kg, respectively
Group 3 (Vitamin D group):
Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to vitamin D in a single intramuscular high-dose (300,000 IU) which was given to all patients regardless patient's age
Group 4 (NAC + Vitamin D group):
Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to both vitamin D and NAC, in the same doses as groups (2 and 3)
Study tools:
Data collection:
A sheet will be constructed for every patient including the following collected data:
(a) History taking:
- Socio-demographic data:
- These include data regarding age, sex, and residence. (b) Intoxication data:
- Type of corrosive substance (acid or alkali).
- Manner of poisoning, whether suicidal, accidental, or criminal.
- Time elapsed between corrosive ingestion and arrival to PCC-ASUH (Delay time).
- Past medical history. (b) Clinical examination
- General examination:
- Vital data including blood pressure, pulse, respiratory rate, and temperature.
- Systemic examination:
- Chest and abdominal examination
- Symptoms (e.g., lip edema, tongue ulcers, vomiting, dysphagia, salivation, and others). (C) Investigations:
- Laboratory investigations:
Both arterial and venous blood samples will be obtained, under complete aseptic condition, for performing the following investigations on admission, 24 hours, and 48 hours after receiving the treatment.
- Arterial blood gas analysis.
- Random blood glucose.
- Serum electrolytes (sodium and potassium).
- Liver enzymes (ALT and AST).
- Renal function tests (Serum urea and creatinine).
- Complete blood count. The neutrophil to lymphocyte ratio and the platelet to lymphocyte ratio will be calculated by dividing the absolute count of neutrophils and platelets, respectively, over the absolute count of lymphocytes (Siddique et al., 2021).
- C-reactive protein (CRP).
II) Radiological investigations:
- Plain chest and abdominal radiograph will be carried out at the time of admission.
- Barium swallow and meal will be done 21 days after acute corrosive ingestion.
- Conditions
- Corrosive Injury
- Being tested
- N Acetyl Cysteine, Vitamin D (Cholecalciferol ), control group
- Keywords
- corrosive ingestion, vitamin D, N acetyl cysteine
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
N Acetyl CysteineDrug
Also called Acetyle cysteine, Hidonac
N-acetyl cysteine (NAC) has a well-established safety profile, its remarkable antioxidant and anti-inflammatory capacity is the biochemical basis used to treat several diseases related to oxidative stress and inflammation. The primary role of NAC as an antioxidant stems from its ability to increase the intracellular concentration of glutathione (GSH), which is responsible for cellular redox imbalance .
It is assumed that NAC acts as a reductant of disulfide bonds, a scavenger of reactive oxygen species and/or a precursor for glutathione biosynthesis N-acetyl cysteine was observed to be useful in the treatment of esophageal damage associated with corrosive substances and in achieving histopathological improvement in an experimental setting
Vitamin D (Cholecalciferol )Drug
Also called (Cholecalciferol ), osavidin
counteracts the pro-fibrotic signals, such as transforming growth factor-β1 (TGF-β1), through several biochemical mechanisms. This inhibits myofibroblasts activation and extra cellular matrix deposition. In addition, vitamin D reduces the expression of pro-fibrotic target genes The antioxidant effect of vitamin D is between the newest suggested non-calcemic roles of this compound through inducing the expression of several molecules involved in the antioxidant defense system including glutathione, glutathione peroxidase and superoxide dismutase (SOD) and suppressing the expression of NADPH oxidase
control groupDrug
Patients allocated in this group received the standard treatment protocol only according to PCC-ASUH guidelines.
| Study group | Role | What they receive |
|---|---|---|
| control | Active comparator | Patients allocated in this group will receive the standard treatment protocol only according to PCC-ASUH guidelines Receives: Drug: control group |
| N acetyl cysteine group | Active comparator | * Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to NAC with loading dose of 150 mg/kg diluted in 200 ml dextrose 5% or saline over 1 hour, followed by a maintenance dose of 50 mg/kg diluted in 500 ml of dextrose 5% or saline over 4 hours then followed by 100 ml/kg diluted in 1000 ml of dextrose 5% or saline over 16 hours
* Preparation and administration of NAC were adjusted according to the age of the patient. In those >12 years old, total volume (NAC and IV fluid) for the bolus, 4-hour infusion, and 16 hours infusion was 200 ml, 500 ml, and 1 liter, respectively. In children <12 years but over 20 kg, volumes were 100 ml, 250 ml, and 500 ml respectively. In those under 20 kg volumes were 3 ml/kg, 7 ml/kg, and 14 ml/kg respectively Receives: Drug: N Acetyl Cysteine; Drug: control group |
| vitamin D group | Active comparator | Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to vitamin D in a single intramuscular high-dose (300,000 IU) which was given to all patients regardless patient's age Receives: Drug: Vitamin D (Cholecalciferol ); Drug: control group |
| N acetyl cysteine and Vitamin D group | Active comparator | Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to both vitamin D and NAC, in the same doses as groups (2 and 3). Receives: Drug: N Acetyl Cysteine; Drug: Vitamin D (Cholecalciferol ); Drug: control group |
What is being measured
The primary outcome is the main question the study is designed to answer.
Stricture formation
Stenosis of esophygeal lumen or gastric lumen after corrosive ingestion which will be seen in barium swallow and meal
Measured: 21 days after corrosive ingestion
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Nov 2025
- Study start1 Oct 2024
- Primary completion31 Oct 2025
- Study completion1 Dec 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Corrosive InjuryStudies of the same condition, open and under way.
- More trials run by Ain Shams 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 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Factorial
- Model description
- Eighty patients were randomly assigned into four groups (1 control and 3 intervention groups 20 patients each)
- Masking
- Double blind
- Who is masked
- Participant, Care provider
- Enrolment
- 80 participants (actual)
Sponsor and investigators
- Lead sponsor
- Ain Shams University
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
- Investigators
- Eglal H Elawady, Professor of toxicology, Study chair, faculty of medicine - Ain Shams UniversityWalaa G Abdelhamid, Assistant Professor, Study chair, faculty of medicine - Ain Shams University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07229456
- Sponsor's protocol ID
- FAMSU MS 611/2024
- Status last verified
- Nov 2025
- First submitted
- 5 Sep 2025
- Last updated
- 17 Nov 2025
- Results posted
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Yes
Study at a glance
From the registry record, last updated by the sponsor on 17 Nov 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Evaluation of the Role of N Acetyl Cysteine and Vitamin D in Improving Outcomes After Corrosive Ingestion
- ClinicalTrials.gov ID
- NCT07229456
- Acronym / sponsor ID
- FAMSU MS 611/2024
- Conditions
- Corrosive Injury
- Keywords
- corrosive ingestion, vitamin D, N acetyl cysteine
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Active, not recruiting
- Enrolment
- 80 participants (actual)
- Lead sponsor
- Ain Shams UniversityUniversity, hospital or other
- Study start
- 1 Oct 2024 (actual)
- Primary completion
- 31 Oct 2025 (actual)
- Study completion
- 1 Dec 2025 (estimated)
- First posted
- 17 Nov 2025 (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 N acetyl cysteine and vitaminD work to improve outcomes after corrosive ingestion in children.
The main questions it aims to answer are:
Does N acetyl cysteine and vitamin D decrease incidence of strictures after corrosive ingestion in children.
Researchers will compare the effect of N acetyl cysteine and vitamin D in decreasing complication , length of hospital stay and start of complete oral intake Eighty patients were randomly assigned into four groups (1 control and 3 intervention groups 20 patients each)
Group 1 (Control group):
- Patients allocated in this group received the standard treatment protocol only according to PCC-ASUH guidelines
Group 2 (NAC group):
- Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to NAC with loading dose of 150 mg/kg diluted in 200 ml dextrose 5% or saline over 1 hour, followed by a maintenance dose of 50 mg/kg diluted in 500 ml of dextrose 5% or saline over 4 hours then followed by 100 ml/kg diluted in 1000 ml of dextrose 5% or saline over 16 hours
Group 3 (Vitamin D group):
Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to vitamin D in a single intramuscular high-dose (300,000 IU) which was given to all patients regardless patient's age
Group 4 (NAC+Vitamin D group):
Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to both vitamin D and NAC, in the same doses as groups (2 and 3
Detailed description
The current study is a controlled randomized, single-blinded clinical trial, conducted on acutely poisoned patients with confirmed history of corrosive ingestion who were admitted to the Poison Control Center, Ain Shams University Hospitals (PCC-ASUH) The required sample size is 80 patients, 20 patients in each group according to the recommendation of statistics committee (Community Medicine, Environmental, and Occupational Medicine Department - Faculty of Medicine, Ain shams University)
Eighty patients were randomly assigned into four groups (1 control and 3 intervention groups 20 patients each)
Group 1 (Control group):
- Patients allocated in this group received the standard treatment protocol only according to PCC-ASUH guideline This included patient stabilization, maintaining patent airways, oxygen administration and ventilatory support when necessary.
In patients presenting with oral symptoms such as lip edema, excessive drooling (sialorrhea), or oral ulcers, the child was kept NPO to prevent further irritation. Topical treatments including antibiotics, anti-inflammatory agents, and antifungals were applied to manage local infection and inflammation.
Intravenous fluids were started to maintain hydration, with the volume calculated based on the Holliday-Segar method as follows: 100 mL/kg for the first 10 kg of body weight, 50 mL/kg for the next 10 kg, and 20 mL/kg for any weight above 20 kg. Fluid selection depended on the clinical condition where isotonic fluids such as 0.9% saline were often used initially, followed by hypotonic solutions containing dextrose and electrolytes for maintenance to prevent complications like hyponatremia or fluid overload Corticosteroids, especially dexamethasone, were administered when there was severe lip edema or suspected airway swelling to reduce inflammation and to prevent airway compromise. The typical dose used was 0.6 mg/kg, up to a maximum of 10 mg. However, steroids were avoided in children presenting with hematemesis or melena, due to the risk of worsening gastrointestinal bleeding.
In cases with GIT symptoms, supportive care was provided. If vomiting was present, ondansetron was administered at a dose of 4 mg every 8 hours until symptoms were controlled, and then on demand. To treat esophagitis and abdominal discomfort, proton pump inhibitors (PPIs) such as omeprazole were used to reduce acid secretion and promote healing of the mucosa. Omeprazole was given at 0.4-0.8 mg/kg, either every 12 or 24 hours, depending on symptom severity.
For children with signs of upper GI bleeding such as hematemesis or melena, urgent resuscitation was initiated. This included blood transfusion in cases of hemoglobin drop, fresh frozen plasma, IV PPI infusion, and hemostatic agents like tranexamic acid (Kapron), etamsylate (Dicynone), and vitamin K (Konakion). Diagnostic imaging such as chest X-ray, erect and supine abdominal X-rays, and abdominal ultrasound were performed to assess complications like perforation or effusion.
In children with respiratory symptoms, especially those with stridor or laryngeal edema, adrenaline was administered to reduce airway swelling. If chemical pneumonitis was suspected, inhaled bronchodilators (e.g., salbutamol every 4-6 hours), mucolytics like N-acetyl cysteine (NAC) or hypertonic saline every 6 hours, and antibiotics (based on culture and sensitivity) were given. Additionally, IV paracetamol at 10-15 mg/kg every 6 hours was used for fever, pain, and inflammation.
For patients who developed dysphagia and could not tolerate oral or enteral feeding for more than 3-5 days, total parenteral nutrition (TPN) was initiated to prevent malnutrition and support tissue healing. TPN was carefully tailored to the child's age, weight, and clinical status. Fluid needs were typically 100-150 mL/kg/day. Glucose, the main energy source, was started at 6-8 mg/kg/min in neonates (up to 12-14 mg/kg/min as tolerated) and 5-10 mg/kg/min in older children. Amino acids, essential for growth and repair, were given at 2-3 g/kg/day in neonates and 1-2 g/kg/day in older children. Lipids were started early at 1-2 g/kg/day, increasing to 3 g/kg/day if needed, particularly in neonates.
Electrolyte supplementation was guided by lab values: sodium (2-5 mEq/kg/day), potassium (1-3 mEq/kg/day), calcium (50-100 mg/kg/day of elemental calcium), magnesium (0.25-0.5 mEq/kg/day), and phosphate (1-2 mmol/kg/day). Micronutrients were also essential - daily multivitamins were given (e.g.,1 mL/day for infants, 2-5 mL/day for older children), along with trace elements such as zinc (100-400 mcg/kg/day), copper (20 mcg/kg/day), manganese (1 mcg/kg/day), selenium (2 mcg/kg/day), and chromium (0.14-0.2 mcg/kg /day).
Group 2 (NAC group):
- Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to NAC with loading dose of 150 mg/kg diluted in 200 ml dextrose 5% or saline over 1 hour, followed by a maintenance dose of 50 mg/kg diluted in 500 ml of dextrose 5% or saline over 4 hours then followed by 100 ml/kg diluted in 1000 ml of dextrose 5% or saline over 16 hours
Preparation and administration of NAC were adjusted according to the age of the patient. In those>12 years old, total volume (NAC and IV fluid) for the bolus, 4-hour infusion, and 16 hours infusion was 200 ml, 500 ml, and 1 liter, respectively. In children <12 years but over 20 kg, volumes were 100 ml, 250 ml, and 500 ml, respectively. In those under 20 kg, volumes were 3 ml/kg, 7 ml/kg, and 14 ml/kg, respectively
Group 3 (Vitamin D group):
Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to vitamin D in a single intramuscular high-dose (300,000 IU) which was given to all patients regardless patient's age
Group 4 (NAC + Vitamin D group):
Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to both vitamin D and NAC, in the same doses as groups (2 and 3)
Study tools:
Data collection:
A sheet will be constructed for every patient including the following collected data:
(a) History taking:
- Socio-demographic data:
- These include data regarding age, sex, and residence. (b) Intoxication data:
- Type of corrosive substance (acid or alkali).
- Manner of poisoning, whether suicidal, accidental, or criminal.
- Time elapsed between corrosive ingestion and arrival to PCC-ASUH (Delay time).
- Past medical history. (b) Clinical examination
- General examination:
- Vital data including blood pressure, pulse, respiratory rate, and temperature.
- Systemic examination:
- Chest and abdominal examination
- Symptoms (e.g., lip edema, tongue ulcers, vomiting, dysphagia, salivation, and others). (C) Investigations:
- Laboratory investigations:
Both arterial and venous blood samples will be obtained, under complete aseptic condition, for performing the following investigations on admission, 24 hours, and 48 hours after receiving the treatment.
- Arterial blood gas analysis.
- Random blood glucose.
- Serum electrolytes (sodium and potassium).
- Liver enzymes (ALT and AST).
- Renal function tests (Serum urea and creatinine).
- Complete blood count. The neutrophil to lymphocyte ratio and the platelet to lymphocyte ratio will be calculated by dividing the absolute count of neutrophils and platelets, respectively, over the absolute count of lymphocytes (Siddique et al., 2021).
- C-reactive protein (CRP).
II) Radiological investigations:
- Plain chest and abdominal radiograph will be carried out at the time of admission.
- Barium swallow and meal will be done 21 days after acute corrosive ingestion.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- Double blind (participant, care provider)
- Number of arms
- 4
- Model description
- Eighty patients were randomly assigned into four groups (1 control and 3 intervention groups 20 patients each)
| Arm | Type | Receives |
|---|---|---|
| control | Active comparator | Drug: control groupPatients allocated in this group will receive the standard treatment protocol only according to PCC-ASUH guidelines |
| N acetyl cysteine group | Active comparator | Drug: N Acetyl Cysteine, Drug: control group* Patients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to NAC with loading dose of 150 mg/kg diluted in 200 ml dextrose 5% or saline over 1 hour, followed by a maintenance dose of 50 mg/kg diluted in 500 ml of dextrose 5% or saline over 4 hours then followed by 100 ml/kg diluted in 1000 ml of dextrose 5% or saline over 16 hours * Preparation and administration of NAC were adjusted according to the age of the patient. In those >12 years old, total volume (NAC and IV fluid) for the bolus, 4-hour infusion, and 16 hours infusion was 200 ml, 500 ml, and 1 liter, respectively. In children <12 years but over 20 kg, volumes were 100 ml, 250 ml, and 500 ml respectively. In those under 20 kg volumes were 3 ml/kg, 7 ml/kg, and 14 ml/kg respectively |
| vitamin D group | Active comparator | Drug: Vitamin D (Cholecalciferol ), Drug: control groupPatients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to vitamin D in a single intramuscular high-dose (300,000 IU) which was given to all patients regardless patient's age |
| N acetyl cysteine and Vitamin D group | Active comparator | Drug: N Acetyl Cysteine, Drug: Vitamin D (Cholecalciferol ), Drug: control groupPatients in this group received the standard treatment protocol according to PCC-ASUH guidelines in addition to both vitamin D and NAC, in the same doses as groups (2 and 3). |
Who may qualify
- Ages
- Up to 18 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult
Key inclusion criteria (1 listed)
- The study included all patients aged from 0 to 18 years old, of both sex, admitted to the PCC-ASUH with confirmed history of corrosive ingestion and exhibiting moderate or severe symptoms (as determined by Poisoning Severity Score 2 or 3, respectively) and DROOL score (Drooling, Reluctance, Oropharynx, Others, and leukocytosis) ≤ 6
Key exclusion criteria (10 listed)
- o Asymptomatic patients.
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 |
|---|---|---|
| N Acetyl CysteineAlso: Acetyle cysteine, HidonacN-acetyl cysteine (NAC) has a well-established safety profile, its remarkable antioxidant and anti-inflammatory capacity is the biochemical basis used to treat several diseases related to oxidative stress and inflammation. The primary role of NAC as an antioxidant stems from its ability to increase the intracellular concentration of glutathione (GSH), which is responsible for cellular redox imbalance . It is assumed that NAC acts as a reductant of disulfide bonds, a scavenger of reactive oxygen species and/or a precursor for glutathione biosynthesis N-acetyl cysteine was observed to be useful in the treatment of esophageal damage associated with corrosive substances and in achieving histopathological improvement in an experimental setting | Drug | N acetyl cysteine and Vitamin D group, N acetyl cysteine group |
| Vitamin D (Cholecalciferol )Also: (Cholecalciferol ), osavidincounteracts the pro-fibrotic signals, such as transforming growth factor-β1 (TGF-β1), through several biochemical mechanisms. This inhibits myofibroblasts activation and extra cellular matrix deposition. In addition, vitamin D reduces the expression of pro-fibrotic target genes The antioxidant effect of vitamin D is between the newest suggested non-calcemic roles of this compound through inducing the expression of several molecules involved in the antioxidant defense system including glutathione, glutathione peroxidase and superoxide dismutase (SOD) and suppressing the expression of NADPH oxidase | Drug | N acetyl cysteine and Vitamin D group, vitamin D group |
| control groupPatients allocated in this group received the standard treatment protocol only according to PCC-ASUH guidelines. | Drug | N acetyl cysteine and Vitamin D group, N acetyl cysteine group, control, vitamin D group |
Primary outcome
Stricture formation
Time frame: 21 days after corrosive ingestion
Stenosis of esophygeal lumen or gastric lumen after corrosive ingestion which will be seen in barium swallow and meal
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 17 Nov 2025.
- Individual participant dataSharing planned: Yes
Related trials for Corrosive Injury
Not yet recruitingObservational study
Relation Between Inflammatory Responses and Sequelae of Pediatric Corrosive Ingestion Cases in Assiut
Corrosive Injury
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.
Eglal H Elawady, Professor of toxicology study chair
faculty of medicine - Ain Shams University
Walaa G Abdelhamid, Assistant Professor study chair
faculty of medicine - Ain Shams University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing N Acetyl Cysteine and Vitamin D (Cholecalciferol ) in people with Corrosive Injury, run by Ain Shams 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 10 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: under way, not looking for participants, as of the sponsor's last update on 17 Nov 2025. 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 phase mean?
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?
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?
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?
Stricture formation (time frame: 21 days after corrosive ingestion). 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 17 Nov 2025.