Glucomannan for the Treatment of Abdominal Pain-related Functional Gastrointestinal Disorders in Childhood
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|ClinicalTrials.gov Identifier: NCT01495806|
Recruitment Status : Completed
First Posted : December 20, 2011
Last Update Posted : June 13, 2013
Background: Functional abdominal pain disorders (FAPD) are common in school-aged children; however, there is no reliable treatment.
Aim: To determine the efficacy and safety of glucomannan for treating FAPD in children.
Trial Setting: Department of Pediatrics, The Medical University of Warsaw.
Intervention: Patients will be enrolled in a double-blind, randomized controlled trial in which they will receive either glucomannan (10g) or placebo for 4 weeks.
|Condition or disease||Intervention/treatment||Phase|
|Functional Gastrointestinal Disorders||Drug: Glucomannan Drug: placebo||Phase 4|
According to the Rome III criteria, abdominal pain-related functional gastrointestinal disorders (FGD) in children may be categorised as functional dyspepsia (FD), irritable bowel syndrome (IBS), abdominal migraine and functional abdominal pain (FAP). Because of their obscure pathophysiology, management of abdominal pain-related FGD remains difficult, prompting interest in new and safe treatment options.Glucomannan is a prebiotic which is nondigestible food ingredients that beneficially affect the host by selectively stimulating the growth and ⁄ or activity of bacteria already resident in the colon. Up to now there has been published one randomized controlled trial which showed that treatment with the prebiotic (trans-galactooligosaccharide), which induced qualitative changes in the faecal flora, was associated with significant changes in stool consistency, flatulence, composite scores (abdominal pain ⁄ discomfort, bloating ⁄ distension and bowel movement difficulty) as well as subjective global assessment values in adult patients with irritable bowel syndrome. These findings suggest that the prebiotics has a potential as a therapeutic agent in functional gastrointestinal disorders.
Methods Patients will be recruited from children referred to the Department of Pediatrics, The Medical University of Warsaw. Each potentially eligible patient will be evaluated by a full review of their clinical history and physical examination. Subjects will receive a questionnaire to record the frequency and severity of pain, drug use and any symptoms they considered important for the last 4 weeks. Patients will be considered for study inclusion, if they will be 8-18 years of age and will have an abdominal pain - related disorder (i.e. (functional dyspepsia, irritable bowel syndrome or functional abdominal pain ( FD or IBS or FAP) classified according to the Rome III diagnostic criteria. Patients with organic gastrointestinal disease (as established by medical history, complete blood count, urinalysis, stool examination for occult blood, ova and parasites, blood chemistries, abdominal ultrasound, breath hydrogen testing and endoscopy, if needed),other chronic disease, growth failure will be excluded from the study. A total of 90 children who will fulfill the Rome III criteria for functional dyspepsia (FD), or irritable bowel syndrome (IBS), or functional abdominal pain (FAP) will be enrolled in a double-blind, randomized controlled trial in which they will received either glucomannan 10g (n = 45), or placebo (n = 45) for 4 weeks. At the end of the study patients will fulfill the questionnaire assessing the outcome measures. The primary outcome measure is treatment success defined as no pain (a relaxed face, score of 0, on the Faces Pain Scale) at the end of the intervention. The secondary outcome measures are (i) improvements in self-reported severity of pain defined as a change in by at least two faces scores measured on the Faces Pain Scale; (ii) self-reported frequency of pain during the preceding month; (iii) use of medication for abdominal pain and (iv) school absenteeism because of abdominal pain.(v)adverse events during the study period.
Statistical Methods The statistical analyses will be conducted with StatsDirect. The Mann-Whitney U test will be used to compare the means of continuous variables if non-normal distribution will be assessed. Proportions will be compared with the Fisher exact test. The difference in study groups was considered significant when the P value will be <.05. the results of this study will be analyzed on the basis of intention to treat.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||90 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||Glucomannn for the Treatment of Abdominal Pain-related Functional Gastrointestinal Disorders in Childhood Randomized Double Blind Placebo Controlled Trial|
|Study Start Date :||January 2010|
|Actual Primary Completion Date :||January 2012|
|Actual Study Completion Date :||January 2012|
5 g 2x 10 day
2 x 5g
|Placebo Comparator: Placebo||
glucose 5 g
- number of patients with no abdominal pain at the end of the study [ Time Frame: 4 weeks (study period) ]
- number of patients with improvement in self-reported severity of pain [ Time Frame: 4 weeks study period ]improvement in self-reported severity of pain is defined as at least two Faces Pain Score improvement at the end of the study compared to the baseline
- number of patients suffered from abdominal pain < 1/week [ Time Frame: 4 weeks (during the study period) ]self reported with questionnaire
- number of patients who used medication for abdominal pain [ Time Frame: 4 weeks study period ]self reported assessed with questionnaire
- number of patients who lost min.1 school day because of abdominal pain [ Time Frame: 4 weeks (study period) ]self reported with the questionnaire
- Number of participants with adverse events as a measure of safety and tolerability [ Time Frame: participants will be followed for the duration of h an expected average of 4 weeks - study period ]self assessed with the questionnaire
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01495806
|Dpt of Pediatrics Warsaw Medical University|
|Warsaw, Poland, 01-410|
|Principal Investigator:||Andrea Horvath, MD||Medical University of Warsaw|