Home › Meningomyelocele › NCT05672849
Safety and Efficacy of Devices Used in Fetoscopic Neural Tube Defect Repair Cases
Recruiting
Who can join
Ages 18 and older · Women
Full eligibility criteria
Inclusion Criteria: * Patients who elect to undergo fetoscopic neural tube defect repair Exclusion Criteria: * Patients who do not elect to undergo fetoscopic neural tube defect repair
About the study
The purpose of the study is to evaluate the safety and efficacy of devices used in patients undergoing fetoscopic neural tube defect repair.
What is being tested
- Modified Surgical Instruments/Devices (Sheaths and Irrigator) (device)
Sponsor: Michael A Belfort · Participants: 100 · Started: Nov 14, 2022
Contact the study team
- Michael A Belfort, MD · Phone: 832-826-7375
- Becky Johnson · Phone: 832-826-7451
Official record on ClinicalTrials.gov — NCT05672849
Locations in the U.S.
| Texas | Texas Childrens Hospital - Pavilion for Women, Houston |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.