Trials / Not Yet Recruiting
Not Yet RecruitingNCT07105267
Open Label Phase IIa Trial Evaluating the Effect and Safety of Transplantation of Fecal Microbiota in Children With Autism Spectrum Disorders and Gastrointestinal Symptoms
A Proof of Concept Study : Open Label Phase IIa Trial Evaluating the Effect and Safety of Transplantation of Fecal Microbiota in Children With Autism Spectrum Disorders and Gastrointestinal Symptoms
- Status
- Not Yet Recruiting
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 5 (estimated)
- Sponsor
- Assistance Publique - Hôpitaux de Paris · Academic / Other
- Sex
- All
- Age
- 36 Months – 72 Months
- Healthy volunteers
- Not accepted
Summary
Autism Spectrum Disorders (ASD), affect approximately 1% of the general population and are characterized by impairments in social communication associated with repetitive/stereotyped behaviors. Approximately one-third of these patients display gastrointestinal (GI) symptoms, and a growing number of studies suggest abnormalities of gut microbiota in ASD. Gut microbiota and the brain interact through complex pathways. Preliminary evidence in adults with ASD suggests that modulation of the gut microbiota by probiotics and/or prebiotics and more recently by fecal microbiota transplantation could improve GI symptoms but also socio-communication deficit, with persistent improvement at year 2.
Detailed description
1. Screening : Screening will be done in ASD units of child psychiatry departments of Robert Debré 2. Information of patients and their families Information will be delivered in the child psychiatry department of Robert Debré hospital. 3. Inclusion Consent will be collected in CIC of Robert Debré hospital during the initial visit by child psychiatrist 7 to 15 days after information from the patient's family. 4. Patient follow-up during trial Initial visit: for parents and patient information. Further visits (W4, W18, W24, M12): treatment administrations will be done at the CIC. Subjects will be evaluated on efficacy and safety and acceptability. Stool, urine and blood samples will be collected. Phone visits (W11 and M9): Safety and the Acceptability questionnaire (parents) will be evaluated. 5. Products: donor and transplant preparation 6. Same administration schedule in FMT * D1 to D4: Vancomycin (10mg/kg, 4 times a day). 1st dose in the CIC, the 3 others at home * D4: Picoprep® treatment at home * D5: First FMT using rectal enema (100ml = 25g of stool from donor) using Foley probe (rectal administration) in CIC * D12: Second FMT using rectal enema (100ml = 25g of stool from donor) using Foley probe (rectal administration) in CIC * D19: Third FMT using rectal enema (100ml = 25g of stool from donor) using Foley probe (rectal administration) in CIC
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | FMT Protocol | FMT protocol Samples (urine, blood, stool) collection Psychological examination Pediatric quality of life Scale Bristol Stool form Scale |
Timeline
- Start date
- 2025-09-01
- Primary completion
- 2027-04-01
- Completion
- 2027-04-01
- First posted
- 2025-08-05
- Last updated
- 2025-08-05
Locations
1 site across 1 country: France
Source: ClinicalTrials.gov record NCT07105267. Inclusion in this directory is not an endorsement.