RecruitingNot Applicable

Safety and Efficacy of Devices Used in Fetoscopic Neural Tube Defect Repair Cases

United States100 participantsStarted 2022-11-14

Plain-language summary

The purpose of the study is to evaluate the safety and efficacy of devices used in patients undergoing fetoscopic neural tube defect repair.

Who can participate

Age range18 Years

SexFEMALE

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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

What they're measuring

Number of adverse events

Timeframe: Immediate Post-Procedure period (until the leave the OR)

Number of device defects, malfunctions, or failures

Timeframe: Immediate Post-Procedure period (until the leave the OR)

Trial details

NCT IDNCT05672849

SponsorMichael A Belfort

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2027-12

Contact for this trial

Michael A Belfort, MD

832-826-7375 belfort@bcm.edu

View on ClinicalTrials.gov More Neural Tube Defects trials