Probiotic for the Prevention of Functional Disorders in Childhood

The recruitment status of this study is unknown because the information has not been verified recently.
Verified August 2012 by University of Bari.
Recruitment status was  Not yet recruiting
Sponsor:
Information provided by (Responsible Party):
Ruggiero Francavilla, University of Bari
ClinicalTrials.gov Identifier:
NCT01671137
First received: August 16, 2012
Last updated: August 20, 2012
Last verified: August 2012
  Purpose

The present study has several aims:

  1. Establish whether Lactobacillus Rhamnosus Strain GG is able to prevent the onset of IBS in a high risk group of children enrolled after an acute gastroenteritis (the study has been powered to this aim).
  2. Establish whether Lactobacillus Rhamnosus Strain GG is able to stabilize the intestinal microbiota after an acute gastroenteritis.
  3. Define the intestinal microbiota of children following an acute gastroenteritis and identify, if possible, a modification of the microbiota that can predict the emergence of Irritable Bowel Syndrome.

Condition Intervention
Gastroenteritis
Other: Lactobacillus Rhamnosus Strain GG

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Prevention
Official Title: A Randomized Controlled Trial of Lactobacillus Rhamnosus Strain GG for The Prevention of Functional Abdominal Pain Children After Acute Gastroenteritis

Resource links provided by NLM:


Further study details as provided by University of Bari:

Primary Outcome Measures:
  • Prevention of Abdominal pain [ Time Frame: 18 months ] [ Designated as safety issue: No ]

    Primary outcome will be the incidence in IBS in children receiving LGG as compared to those receiving placebo. We have chosen pain as the primary outcome measure, in line with the proposed points-toconsider for IBS trials (Corazziari E. Consensus report: Clinical trial guidelines for pharmacological treatment of irritable bowel syndrome. Aliment Pharmcol Ther 2003;18:569).

    IBS or chronic abdominal pain will be diagnosed and categorised according to ROME III criteria (Rasquin A, Di Lorenzo C, Forbes D, et al. Childhood functional gastrointestinal disorders: child/adolescent. Gastroenterology. 2006;130).



Secondary Outcome Measures:
  • Incidence of IBS [ Time Frame: 6 months ] [ Designated as safety issue: No ]
    Evaluation of frequency/severity of symptoms according to treatment arm;

  • Children's health [ Time Frame: 24 months ] [ Designated as safety issue: No ]
    Evaluation of perception of children's health according to parents

  • Intestinal microbiota [ Time Frame: 24 months ] [ Designated as safety issue: No ]
    Investigate the modification of intestinal microbiota.


Estimated Enrollment: 400
Study Start Date: September 2012
Estimated Study Completion Date: September 2014
Estimated Primary Completion Date: July 2014 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Lactobacillus Rhamnosus Strain GG
LGG (6 × 109 colony forming units)
Other: Lactobacillus Rhamnosus Strain GG
Lactobacillus Rhamnosus Strain GG
Other Name: LGG
Placebo Comparator: Placebo
Placebo
Other: Lactobacillus Rhamnosus Strain GG
Lactobacillus Rhamnosus Strain GG
Other Name: LGG

  Hide Detailed Description

Detailed Description:

Study Design A randomized, double-blind, placebo-controlled, parallel-group trial planned following the recommendations established by the Consensus report on clinical trial in IBS.

Children during/after an acute episode of gastroenteritis will enter a 12 months treatment (m1-m12) period followed by a 6 months follow-up phase (m13-m18).

Children will be assigned consecutive numbers, starting with the lowest number available, and randomly assigned, with the use of a computer generated randomisation list using permuted block design, to receive orally either LGG (6 × 109 colony forming units) or placebo (capsules identical in taste and appearance to the active study product except for the absence of LGG) once a day. Enrolled children will be entered sequentially to receive the assigned treatment. Boxes containing placebo will have the same shape, dimension, indication and appearance as those containing the viable LGG and will be provided by the probiotic producer (Dicofarm SpA, Rome, Italy) which ensure that the study is blinded for investigators and patients. Group assignment will be concealed from participants and investigators.

Power calculation With the assumption that, in a 12 month period, IBS would be expected in 16% of children after an episode of acute gastroenteritis as opposed to 5% in the general paediatric population without gastroenteritis, we calculated that a sample of 210 children per group would be required for the study to have 80% power to show an advantage of LGG over placebo in reducing the rate of IBS, based on a two-sided type 1 error rate of 5%..

Eligibility of Patients Patients recruited from primary care paediatricians or paediatric wards during/after (less seven days) an episode of gastroenteritis (bacteria/viruses/parasites).

Inclusion criteria:

  1. Children of 2 - 16 years of age;
  2. Either sex.

Exclusion criteria:

  1. Chronic disease,
  2. Clinical history of abdominal pain history suggestive for functional dyspepsia/aerophagia/abdominal migraine
  3. Growth failure,
  4. Alarm signs of organic conditions.

Assessments, Compliance and Adherence. During the duration of the trial (m1-m18) patients will record gastrointestinal symptoms on monthly bases and the following data will be collected: a) questionnaire of frequency/severity of pain, b) school absence and c) GI symptom score by the compilation of the gastrointestinal symptom rating score.

To assess the severity of pain a combination of the self-report Visual Analogue Scale (VAS) and the Faces Pain Scale (FPS) will be used. The 0-10 mm VAS scale (0 no pain, 10 worst possible pain) included a horizontal colour gradient (green-red), plus a rating. When asked to evaluate pain, the child would point to a level and trace a line. This particular VAS is a validated standard to evaluate pain in children older than five. Assessment was eased coupling the VAS with the FPS that consists of six faces ranging from a relaxed face to a face showing intense pain.

Gastrointestinal symptom rating score (GSRS) consists of a 15-point questionnaire to assess severity and frequency of symptoms validated by Svedlund et al..

During the six months of follow-up the questionnaire will be compiled every other months and the GSRS at month 18.

The impact on parent's overall assessment of treatment will be obtained by a monthly interview by the question "how do you feel the medication is affecting the health of your child?"; possible answers are significant, mild, or no relief.

To ensure compliance one investigator will contact the families every four weeks to monitor the process of the study. Adherence will be measured by counting the number of capsules returned at the study visit; children who missed for more than 20% of the medications were considered noncompliant.

Outcome Measures Primary outcome will be the incidence in IBS in children receiving LGG as compared to those receiving placebo. We have chosen pain as the primary outcome measure, in line with the proposed points-to-consider for IBS trials.

IBS or chronic abdominal pain will be diagnosed and categorised according to ROME III criteria.

Secondary outcomes are: 1) evaluation of frequency/severity of symptoms according to treatment arm; 2) evaluation of perception of children's health according to parents and 3) modification of intestinal microbiota.

Intestinal microbiota The intestinal microbiota will be assesses according to methods published elsewhere.

To define the modification of the intestinal microbiota following an acute gastroenteritis and to determine whether the onset of the IBS is anticipated by a modification of intestinal microbiota we will proceed to the collection of faecal samples at entry, after one month and every two months after enrolment. During the six months of follow-up a fecal sample will be collected only at month 18.

Bacteria DNA in stools will be extracted and stored at -80°C for future analysis. At the end of the trial a subset of informative fecal bacterial DNA will be assessed: a) patients that have NOT developed IBS (LGG and placebo), b) patients that have developed IBS (LGG and placebo).

The analysis of the intestinal microbiota of these informative cases will help to assess whether there is a intestinal microbiota suggestive of future inset of IBS and ability of LGG to stabilize the intestinal microbiota.

Adverse Events and Disallowed Medication Adverse events were monitored throughout the study. Children will not allowed to consume any probiotic other than those provided (except for a transient period no longer that 2 weeks) and they will be invited to continue their eating and physical exercise habits. Concomitant use of medications affecting gastrointestinal motility and/or pain perception was allowed, providing parents registered the intake.

  Eligibility

Ages Eligible for Study:   3 Years to 16 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Children of 3 - 16 years of age;
  2. Either sex.

Exclusion Criteria:

  1. Chronic disease,
  2. Clinical history of abdominal pain history suggestive for functional dyspepsia/aerophagia/abdominal migraine
  3. Growth failure,
  4. Alarm signs of organic conditions.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01671137

Contacts
Contact: Ruggiero Francavilla 0805592963 rfrancavilla@gmail.com

Locations
Italy
Clinica Pediatrica Active, not recruiting
Bari, Puglia, Italy, 70125
Sponsors and Collaborators
University of Bari
Investigators
Principal Investigator: Ruggiero Francavilla University of Bari
Principal Investigator: Ruggiero FRANCAVILLA DEPARTMENT OF BIOMEDICINA ETA' EVOLUTIVA
  More Information

No publications provided

Responsible Party: Ruggiero Francavilla, MD, PhD, University of Bari
ClinicalTrials.gov Identifier: NCT01671137     History of Changes
Other Study ID Numbers: PrevenDAR, Prevent-001
Study First Received: August 16, 2012
Last Updated: August 20, 2012
Health Authority: Italy: Ethics Committee

Keywords provided by University of Bari:
Lactobacillus GG
Functional Abdominal Pain
Children
Acute
Gastroenteritis

Additional relevant MeSH terms:
Gastroenteritis
Gastrointestinal Diseases
Digestive System Diseases

ClinicalTrials.gov processed this record on October 01, 2014