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NCT05771688 · ClinicalTrials.gov registry record · NA
Fetoscopic Endoluminal Tracheal Occlusion
A NA study of Hernia, DIaphragmatic, Congenital, sponsored by Children's Hospitals and Clinics of Minnesota.
- Recruiting
- Registry status
- NA
- Development phase
- 10
- Enrollment target
- 1
- Study location
NCT05771688: Recruiting NA study of Hernia, DIaphragmatic, Congenital, sponsored by Children's Hospitals and Clinics of Minnesota.
NCT05771688 is a NA study of Hernia, DIaphragmatic, Congenital that is actively recruiting participants, run by Children's Hospitals and Clinics of Minnesota. The registered enrollment target is 10 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05771688, a NA study of Hernia, DIaphragmatic, Congenital, is actively recruiting participants, sponsored by Children's Hospitals and Clinics of Minnesota.
- RECRUITING
- Registry status
- NA
- Development phase
- 10 participants
- Enrollment target
- 1
- Study location
Study Summary
This is a single site pilot trial to study the feasibility of Fetoscopic Endoluminal Tracheal Occlusion (FETO) therapy in the most severe group of fetuses with congenital diaphragmatic hernia (CDH) at Midwest Fetal Care Center, a collaboration between Allina Health and Children's Minnesota. This procedure aims to increase fetal lung volume before birth and improve survival after birth. This study will enroll 10 pregnant people and their baby who meet study criteria.
Primary Outcome
Successful completion of balloon insertion in fetuses with severe CDH defined as direct visualization of balloon above the carina at the time of FETO procedure.
Conditions Studied
Interventions
- DEVICE FETO therapy
Study Locations (1)
Minnesota
- Midwest Fetal Care Center - Minneapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2024-02-22 |
| Est. Completion | 2028-09 |
| Phase | NA |
What NCT05771688 shows while recruiting
NCT05771688 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 1 condition, with Hernia, DIaphragmatic, Congenital appearing as the primary indexed condition, and to 1 intervention - of which FETO therapy is the first listed.
NCT05771688 reports a single indexed study location in Minnesota.
Frequently Asked Questions
What is clinical trial NCT05771688 about?
NCT05771688 is a clinical study titled "Fetoscopic Endoluminal Tracheal Occlusion". This is a single site pilot trial to study the feasibility of Fetoscopic Endoluminal Tracheal Occlusion (FETO) therapy in the most severe group of fetuses with congenital diaphragmatic hernia (CDH) at Midwest Fetal Care Center, a collaboration between Allina Health and Children's Minnesota. This pro...
What is the current status of trial NCT05771688?
This trial is currently recruiting. It is a NA study. The enrollment target is 10 participants. The study started on 2024-02-22. Estimated completion is 2028-09.
What conditions does trial NCT05771688 study?
This clinical trial studies the following conditions: Hernia, DIaphragmatic, Congenital.
What interventions are being tested in trial NCT05771688?
The interventions under investigation include: FETO therapy (DEVICE).
Who is sponsoring clinical trial NCT05771688?
This trial is sponsored by Children's Hospitals and Clinics of Minnesota, which has 31 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05771688 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Hernia, DIaphragmatic, Congenital
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT05771688's enrollment target sits among peer trials
10 1927th of 2000 higher than 26 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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