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Study Protocol for a Randomized Controlled of Fecal Microbiota Transplantation Via Different Routes in Children With Moderate-to-Severe Autism Spectrum Disorder

Status: Recruiting
Location: See location...
Intervention Type: Procedure
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This is a single-center, randomized, double-dummy, triple-blind, placebo-controlled, three-arm parallel-group superiority trial. The study aims to compare the efficacy and safety of Fecal Microbiota Transplantation (FMT) administered via two different invasive routes-nasojejunal tube (NJT) and colonoscopy-versus a placebo control in children aged 3-16 years with moderate-to-severe Autism Spectrum Disorder (ASD). A total of 75 participants will be randomized in a 1:1:1 ratio to receive either active FMT via NJT with sham colonoscopy, active FMT via colonoscopy with sham NJT, or placebo via both routes. All participants will continue their stable behavioral interventions throughout the study. The primary outcome is the change from baseline to Week 24 in the total score of the Childhood Autism Rating Scale (CARS). Secondary outcomes include changes in other behavioral and gastrointestinal symptom scores, gut microbiota profiling, and safety assessments over 48 weeks.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 3
Maximum Age: 16
Healthy Volunteers: f
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• Aged 3-16 years.

• Diagnosed with ASD according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5), with a Childhood Autism Rating Scale (CARS) total score ≥36 (moderate-to-severe autism).

• Legal guardians fully comprehend the trial's informed consent and voluntarily provide written consent.

• Compliance with follow-up visits, examinations, and specimen collection.

• No probiotic supplements consumed within the preceding 3 months.

Locations
Other Locations
China
Children's Hospital, Shenzhen
RECRUITING
Shenzhen
Contact Information
Primary
Dongling Dai, PhD
daidong3529@email.szu.edu.cn
08618938690736
Time Frame
Start Date: 2026-03-21
Estimated Completion Date: 2027-04-12
Participants
Target number of participants: 1
Treatments
Active_comparator: Group 1 (FMT-NJT)
active FMT via nasojejunal tube + sham colonoscopy
Active_comparator: Group 2 (FMT-C)
active FMT via colonoscopy with placement of a transendoscopic enteral tube (TET) secured at the cecum during the first session, followed by two subsequent infusions via the indwelling TET + sham nasojejunal intubation.
Placebo_comparator: Group 3 (Control)
placebo via nasojejunal tube + placebo via colonoscopy (sham procedures for both routes)
Sponsors
Collaborators: Shenzhen Institutes of Advanced Technology ,Chinese Academy of Sciences, Shenzhen Medical Academy of Research and Translation
Leads: Shenzhen Children's Hospital

This content was sourced from clinicaltrials.gov

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