RecruitingNot applicableNCT06739356
North American Fetal Therapy Network for Long-term Outcome Following Fetoscopic Endoluminal Tracheal Occlusion in Severe Left and Right Congenital Diaphragmatic Hernia
Studying Congenital diaphragmatic hernia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- The University of Texas Health Science Center, Houston
- Principal Investigator
- Anthony Johnson, DOThe University of Texas Health Science Center, Houston
- Intervention
- Fetal Treatment arm (FETO Group)(device)
- Enrollment
- 80 enrolled
- Eligibility
- 18 years · FEMALE
- Timeline
- 2025 – 2031
Study locations (1)
- The University of Texas Health Science Center at Houston, Houston, Texas, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT06739356 on ClinicalTrials.govOther trials for Congenital diaphragmatic hernia
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