Chronic Idiopathic Constipation (CIC) Clinical Trials

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Evaluation of the Efficacy and Safety of the Multistrain Probiotic BioAmicus Complete in Improving Gastrointestinal Symptoms in Children Aged 0-24 Months: A Randomized, Open-Label, Parallel-Group, Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Other, Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Infants often experience functional gastrointestinal symptoms (e.g., colic, excessive gas, regurgitation, constipation, or loose stools) that distress families and may reflect an imbalance of the gut microbiome. This study evaluates whether the multistrain probiotic BioAmicus Complete can improve caregiver-reported gastrointestinal symptoms in infants 0-24 months and is safe for use in this population. The primary assessment is the change in the Infant Gastrointestinal Symptom Questionnaire (IGSQ) total score from the start to the end of the study period. Secondary assessments include symptom domains (colic/regurgitation, stool frequency and consistency), caregiver quality of life, growth parameters (weight and length), health care utilization and antibiotic exposure, and overall safety/tolerability (adverse events and serious adverse events). Stool samples will be analyzed to explore changes in the gut microbiome.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 2
Healthy Volunteers: f
View:

• Age 0-24 months at enrollment.

• Infant has clinician-assessed functional gastrointestinal symptoms (e.g., colic/irritability, regurgitation, constipation, loose stools), judged suitable for study participation.

• Parent or legal guardian provides written informed consent and agrees to comply with study procedures (questionnaires/diaries and sample collection, if applicable).

• Caregivers agree to avoid other probiotic products during the study period, except as directed by the study team.

Locations
Other Locations
Viet Nam
Clinical Trial and Bioequivalence Center
RECRUITING
Haiphong
Contact Information
Primary
Nguyen Thi Thu Phuong, MD, PhD
nttphuong@hpmu.edu.vn
+84936685007
Time Frame
Start Date: 2025-09-05
Estimated Completion Date: 2026-05-30
Participants
Target number of participants: 110
Treatments
Experimental: BioAmicus Complete + Usual Care
Participants receive BioAmicus Complete (multistrain probiotic) oral drops in addition to usual care for infant functional GI symptoms. Product is administered by caregivers per protocol/label for 42 days; adherence is recorded. No other probiotic products are permitted during the study. Concomitant medications and routine management are allowed at the investigator's discretion.
Active_comparator: Usual Care Alone
Participants receive standard clinical management per local practice for infant functional gastrointestinal symptoms. No probiotic supplementation is provided (participants are asked to avoid other probiotic products during the study). Concomitant medications and supportive care may be used as clinically indicated at the investigator's discretion.
Sponsors
Leads: Haiphong University of Medicine and Pharmacy

This content was sourced from clinicaltrials.gov