North American Fetal Therapy Network Prospective Registry for Long-term Outcome Following Fetoscopic Endoluminal Tracheal Occlusion in Severe Left and Right Congenital Diaphragmatic Hernia
Part of paid clinical trials in Rochester, Minnesota.
- Sponsor
- Mayo Clinic
- Study ID
- NCT07564297
- Status
- Not Yet Recruiting
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Conditions
- Congenital Diaphragmatic Hernia
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 50 Years
- Healthy Volunteers
- Not accepted
Interventions
- Fetoscopic Endoluminal Tracheal Occlusion — DEVICEMothers who chose to undergo a Fetoscopic Endoluminal Tracheal Occlusion procedure for severe left and right congenital diaphragmatic hernia will be followed until the infant is 2 years of age.
- Standard of Care — OTHERMothers who chose to receive expectant management for severe left and right congenital diaphragmatic hernia will be followed until the infant is 2 years of age.
Study Details
The purpose of this research is to determine if babies who undergo a Fetoscopic Endoluminal Tracheal Occlusion (FETO) procedure survive more often and have less long-term complications than babies who have similarly severe Congenital Diaphragmatic Hernia (CDH) that have not had the FETO procedure performed during pregnancy
Key Dates
- Start date
- Jun 1, 2026
- Status verified
- Apr 2026
- Primary completion
- May 31, 2036
- Completion
- May 31, 2038
Study Design
- Enrollment
- 80 participants (estimated)
Arms
- Arm: FETO Surgery
- Arm: Standard of Care
Primary Outcome Measure
Number of FETO procedure complications [ Time Frame: 2 years ]
Central Contacts
- OB/GYN Clinical Research Team, Krista Storing507-266-3382
- OB/GYN Clinical Research Team, Krista Storing
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Mayo Clinic in Rochester | Rochester | Minnesota | 55905 | - |
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