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NCT Number: NCT07536698

Co-supplementation With Bifidobacterium Longum W11 and Colopectin for Maintenance Therapy in Children With Functional Constipation

Functional constipation is a common condition in children and often requires prolonged maintenance treatment with macrogol. This randomized, double-blind, placebo-controlled trial will evaluate whether co-supplementation with Bifidobacterium longum W11 and Colopectin can support maintenance therapy in children with functional constipation who are receiving macrogol and are candidates for weaning. Participants aged 2 to 6 years will be randomized to receive either the active supplementation or placebo once daily for 4 weeks, followed by 4 weeks of follow-up after treatment discontinuation. The study will assess persistence of constipation after macrogol discontinuation, as well as stool consistency, distress during evacuation, soiling episodes, and treatment compliance.

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Key information

Age range

2 year–6 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

Functional constipation is one of the most common gastrointestinal disorders in childhood and is frequently associated with painful or infrequent defecation, stool retention, and reduced quality of life. In many children, maintenance treatment with macrogol is required for prolonged periods, and gradual weaning may be clinically challenging. Therefore, supportive dietary or microbiota-targeted strategies that may facilitate maintenance management and discontinuation of macrogol are of clinical interest.

Bifidobacterium longum W11 is a probiotic strain with potential effects on intestinal function and motility, while Colopectin contains prebiotic and fiber-related components that may help support bowel regularity. The combination is being investigated as a co-supplementation strategy in children with functional constipation during the maintenance phase of treatment.

This study is a randomized, double-blind, placebo-controlled, parallel-group trial in children aged 2 to 6 years with functional constipation who have been receiving maintenance-dose macrogol for at least 3 months and are candidates for treatment weaning. A total of 100 participants will be randomized in a 1:1 ratio to receive either Bifidobacterium longum W11 (Bowell®) plus Colopectin (Colopectin®) or placebo, administered once daily between meals in the afternoon for 4 weeks. After the treatment period, supplementation will be discontinued and participants will be monitored for an additional 4 weeks.

Clinical assessments will be performed at baseline (T0), at Week 4 (T1), and at Week 8 (T2). The primary endpoint is persistence of constipation, defined as 2 or fewer bowel movements per week, after discontinuation of macrogol therapy. Secondary endpoints include changes in stool consistency assessed using the Bristol Stool Scale, presence or absence of distress during evacuation, number of soiling episodes, and treatment compliance.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Children aged 2 to 6 years
  • Diagnosis of functional constipation
  • Receiving maintenance therapy with macrogol for at least 3 months
  • Candidates for weaning from macrogol therapy

Exclusion criteria

  • Children with intestinal meteorism or flatulence
  • Children diagnosed with organic constipation
  • History of previous abdominal surgery
  • Children with frailty or disabilities
  • Presence of other organ diseases or syndromes

Treatment and study plan

Bifidobacterium longum W11 (Bowell®) + Colopectin (Colopectin®)

Dietary Supplement

Combination of probiotic (Bifidobacterium longum W11) and prebiotic components (Colopectin) administered in sachet form once daily between meals in the afternoon.

Placebo

Other

Placebo composed of corn starch, matched in appearance and administration schedule to the active intervention.

Primary outcomes

  1. Persistence of Constipation After Discontinuation of Macrogol Therapy

    Time frame: Week 8

    Persistence of constipation defined as 2 or fewer bowel movements per week after discontinuation of macrogol therapy.

Secondary outcomes

  1. Change in Stool Consistency (Bristol Stool Scale)

    Time frame: Baseline, Week 4, and Week 8

    Change in stool consistency assessed using the Bristol Stool Scale between baseline (T0), Week 4 (T1), and Week 8 (T2).

  2. Presence of Distress During Evacuation (Caregiver-Reported Assessment)

    Time frame: Baseline, Week 4, and Week 8

    Assessment of presence or absence of distress during defecation based on caregiver or parent report recorded during clinical evaluation.

  3. Number of Soiling Episodes

    Time frame: Baseline, Week 4, and Week 8

    Number of episodes of fecal soiling during the study period.

  4. Participant Compliance With Assigned Intervention (Caregiver-Reported Administration)

    Time frame: Week 4

    Assessment of participant compliance with the assigned intervention based on caregiver or parent report of administration of the study product during the treatment period.

Study contacts

Contact information is provided by the study sponsor or research team.

Dr Amjad Khan, DPhil

CONTACT

[email protected]

Francesco Valitutti, MD, PhD

CONTACT

[email protected]

+39 392 232 2182

Sponsors and collaborators

Lead sponsor

Liaquat University of Medical & Health Sciences

Other

Collaborators

  • Università degli Studi dell'Insubria

Registry information

Official study title

Efficacy of Co-supplementation With Bifidobacterium Longum W11 and Colopectin in the Maintenance Therapy of Children With Functional Constipation: A Randomized Double-Blind Placebo-Controlled Trial

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Apr 17, 2026
Registry last updated
Apr 17, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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