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Intra-rectal Botulinum Toxin Injection for Intractable Non-retentive Fecal Incontinence in Children - an Open Label Pilot Study

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Early Phase 1
SUMMARY

Background: Fecal Incontinence (FI) is a frustrating and prevalent GI condition with profound social implications and a marked effect on quality of life. Treatment options are limited for children whose FI is not secondary to constipation (overflow incontinence), and they are defined as having non-retentive fecal incontinence (NRFI). Rectal botulinum injections (RBI) have recently shown promise for the treatment of FI in adults, following a large, randomized placebo-controlled trial, but no data exists regarding efficacy in children.

Objectives: To evaluate the efficacy and safety of RBI in children with non-retentive fecal incontinence.

Methods: A prospective open-label pilot study. Children with intractable NRFI will be screened using anorectal manometry and a colonic transit study. Eligible patients will receive one course of RBI and data regarding FI frequency will be prospectively collected during a 15-week period. Significance: New treatment options for children with intractable fecal incontinence are highly in need. The current study aims to introduce a new treatment modality into pediatric research and patient care.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 4
Maximum Age: 18
Healthy Volunteers: f
View:

• Children 4-18 years old with fecal incontinence for a period greater than 6 months.

• FI frequency of ≥ 3 episodes/week.

• After appropriate medical evaluation, FI cannot be explained by another medical condition.

• Normal colonic transit study, defined as passage of 80% of markers on day

• Normal RAIR on anorectal manometry

Locations
Other Locations
Israel
Shaare Zedek Medical Center
RECRUITING
Jerusalem
Contact Information
Primary
Dotan Yogev, MD
dotany@szmc.org
97225645027
Backup
Zivia Shavit, MSc
zivias@szmc.org.il
972542520204
Time Frame
Start Date: 2025-07-01
Estimated Completion Date: 2030-09
Participants
Target number of participants: 14
Treatments
Experimental: Botulinum toxin
Related Therapeutic Areas
Sponsors
Leads: Shaare Zedek Medical Center

This content was sourced from clinicaltrials.gov