The Effectiveness of Pleuran in Treatment of Acute Gastroenteritis in Children

Study design: This will be a randomized, fully-blind, placebo-controlled trial, with allocation 1:1.

Study population: Children aged 13- 120 months, hospitalized or requiring a visit to the emergency department due to acute gastroenteritis (AGE) lasting at least 24 h, but no longer than 72 h at the time of inclusion to the study.

The setting of the study: The study participants will be recruited from patients requiring hospitalization in 4 paediatric departments or counselling in the emergency department (ED) due to AGE in the Paediatric Teaching Clinical Hospital, the Medical University of Warsaw.

Pre-intervention assessment:

We will evaluate the inclusion and exclusion criteria of the study within 24 hours of hospitalization or ED visit basing on the physical examination and interviews with caregivers. The BMI will be calculated and put on WHO percentiles charts. In order to determine the etiology of AGE, the stool sample will be collected for viral tests (rota-, adeno- and noroviruses markers) before the intervention. If any indication for microbiological stool investigation occurs (the patient in severe condition or with prolonged symptoms in whom specific treatment is considered, or patient with underlying chronic disease), the stool sample will be cultured. The caregivers will be informed about the purpose, methods, safety of the intervention and the course of the study. In order to ensure that the assessed parameters and endpoints are comparable appropriate scales will be applied. To assess the severity of diarrhea, the Modified Vesikari Score will be used. The dehydration degree will be evaluated by means of the WHO scale and the Clinical Dehydration Scale (CDS) recommended by the European Society for Paediatric Gastroenterology, Hepatology and Nutrition (ESPGHAN). The Bristol Stool Form Scale will help to objectify the assessment of stool consistency.

Randomization:

The randomization will involve the random allocation of patients to group A or B. The stratified randomization has been designed with the use of two subgroups. The subgroups will be created depending on the duration of diarrhea at the time of enrolment: 24-48 h (short-lasting diarrhea- SLD) and 48-72 h (long-lasting diarrhea- LLD). The participants of each subgroup will be randomly allocated to the study groups (experimental or control), in blocks of four.

Allocation concealment and blinding:

The active product and placebo will be prepared, weighed, packaged in identical bottles and signed with random numbers by the manufacturer, with the blinded meaning of numbers. The information about the allocation will be deposited in a sealed envelope in a safe place in the administrative part of the department, kept by the independent person not involved in the study. The study product will be delivered to the main researcher in boxes of four, ensuring the contest of 2 active and 2 placebo samples in each box. Subsequent boxes will be used to allocate consecutive patients within the subgroups A and B. By opening each subsequent box, the numbers of bottles in the box will be randomly assigned to the next four patients in a subgroup by the researcher. The contents of the bottles will look and taste the same. Researchers, caregivers, patients, and a person responsible for the statistical analysis will be blinded to the intervention until the completion of the study.

Intervention:

Children allocated to the experimental group will receive Imunoglukan PH4 oral suspension (10 mg of pleuran and 10 mg of vitamin C in 1 ml of syrup) in a dose 1 ml / 5 kg body weight, while patients in the control group will receive a placebo: a vitamin C oral suspension (10 mg of vitamin C in 1 ml of syrup) in a dose 1 ml / 5 kg body weight. Both syrups will be administered once a day in the morning, before the first meal, until signs of AGE subside (< 3 stools / 24 hours and normalization of stool consistency - grade 2-5 according to Bristol Stool Form Scale) or until the 14th day of the intervention.

Concomitant treatment:

To ensure proper rehydration, patients in both groups will receive an oral rehydration solution (ORS) or intravenous fluids if necessary, according to daily fluids requirements. A normal diet will be delivered. Each patient will receive antipyretic, analgesic (Ibuprofen, Acetaminophen), and antiemetic (Ondansetron) if necessary. Patients will not receive other medicines that may interfere with the disease course (probiotics, Diosmectite, Racecadotril). If indications occur, the patient will receive an antibiotic according to the ESPGHAN recommendations

Follow up:

During hospitalization, patients will be examined every day by the physician, with the assessment of dehydration level, the need for intravenous rehydration or concomitant treatment. The results of the evaluation will be recorded in the Case Report Form (CRF). Both during and after the hospitalization, the caregiver will record AGE symptoms in a diary (a number of stools per day, their consistency and accompanying symptoms e.g. fever, vomiting, abdominal pain). Complete diaries will be collected from caregivers via email or by telephone conversation. After discharge, caregivers will have the possibility to contact a physician to receive basic consultation about oral rehydration and eventual side effects.

Data management:

Coded, paper CRF containing all the scales and questionnaires will be created for each patient. After finishing the observation, the data from the symptoms diaries completed by the caregivers will be transferred by the physician to the paper versions of the CRFs. After completing the study, data from the CRFs will be transferred to two electronic databases by two independent persons to confirm the accuracy of the data. Electronic database and CRFs will be prepared in Statistical Analysis System (SAS) software. The collected data will be properly stored to allow for data verification. Confidentiality of data, including personal data of the study participants, will be maintained.

Adverse events (AE) Every AE will be recorded and reported to the investigator and manufacturer, according to a pre-established procedure.

Sample size:

The Altman nomogram was used to estimate the sample size of experimental and control groups. To demonstrate a clinically relevant difference of 24 h in duration of AGE symptoms in experimental and control groups, with 5% significance level and a power of 90%, assuming the standard deviation of the variable in each group of 40 h, a sample of 110 patients will be needed (55 patients in each group). Allowing for 10% attrition of participants during the study, we estimated the sample size as 120 patients (60 patients for each experimental and control group).

Statistical analysis:

Descriptive statistics will be used to summarise baseline characteristics. Intention-to-treat (ITT) and per protocol analyses will be used to present the results of the study. The comparison of group A and B in terms of the primary endpoint (duration of diarrhea) will be performed with Student's t-test if the p-value of the Shapiro-Wilk test will be >0.05. Otherwise, the Mann-Whitney U test will be used. In the case of dropouts or not completed observations before the 14th days of the study, the log-rank test will be performed. The Chi-squared test or Fisher's exact test will be used to compare the groups A and B in terms of the incidence of adverse events and the severity of diarrhea. Statistical significance will be based on two-tailed tests with p-value of 5%. All estimates will be presented with 95% confidence interval.

Amendment No 1:

The presented protocol contains amendments approved by the Bioethics Committee on May 11, 2020. The main reason for those changes was an unsatisfactory pace of recruitment in the first 11 months of study commencement. A detailed analysis revealed the reduction in the number of hospitalizations due to AGE in our Department compared to the previous year and difficulties in meeting the inclusion criteria. In the following months, the COVID pandemic significantly limited the number of patients hospitalized in our hospital. By the time the changes were made we recruited only three patients into the study.

For the listed reasons we have introduced the following changes to the protocol:

1. The first version of the protocol assumed the recruitment of patients among hospitalized children only. The amendment introduced the possibility of recruitment also among children requiring counselling in the emergency department.
2. Initially, patients were recruited only at the Department of Pediatric with Clinical Assessment Unit (the unit initiating and conducting the study). The amendment introduced 4 other clinics of the Pediatric Teaching Clinical Hospital, the Medical University of Warsaw, including the Emergency Department.
3. The age group of recruited patients initially 13- 60 months (up to 6 years of age) was extended to older children 13- 120 months (up to 10 years of age).

Amendment No 2

The presented protocol contains amendments approved by the Bioethics Committee on December 13, 2021. The main reason for those changes was an unsatisfactory pace of recruitment, caused by a significant change in the profile of hospitalized patients due to the SARS-CoV2 pandemic. By the time the changes were made we recruited only ten patients into the study.

1. The amendment introduced two other locations for patient recruitment: The Department of Pediatrics of Warsaw Children's Hospital and The Department of Pediatrics of Hospital of Trzebnica, Poland.
2. The amendment introduced the possibility of recruitment among children requiring outpatient counseling due to acute diarrhea.