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NCT06444347 · ClinicalTrials.gov registry record · NA
Impact of Biosynthetic Mesh on Paraesophageal Hernia Repair
A NA study of Hiatal Hernia, sponsored by Weill Medical College of Cornell University.
- Recruiting
- Registry status
- NA
- Development phase
- 200
- Enrollment target
- 6
- Study locations
NCT06444347: Recruiting NA study of Hiatal Hernia, sponsored by Weill Medical College of Cornell University.
NCT06444347 is a NA study of Hiatal Hernia that is actively recruiting participants, run by Weill Medical College of Cornell University. The registered enrollment target is 200 participants, below the 868-participant average among 9 other Hiatal Hernia trials with a reported enrollment target (77% lower). The trial reports 6 study locations across 4 states. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT06444347, a NA study of Hiatal Hernia, is actively recruiting participants, sponsored by Weill Medical College of Cornell University.
- RECRUITING
- Registry status
- NA
- Development phase
- 200 participants
- Enrollment target
- 6
- Study locations
Study Summary
The aim of this study is to find out if using a certain kind of mesh can reduce the chances of hiatal hernias coming back after anti-reflux surgery. Participants undergoing antireflux surgery will be assigned to one of two groups, a group that has surgery with mesh, or a group that has surgery without mesh.
Conditions Studied
Interventions
- DEVICE Biosynthetic Mesh
- PROCEDURE Hiatal Hernia Repair
Study Locations (6)
New York
- NYU Langone Health - New York
- Weill Cornell Medicine - New York
- Lenox Hill Hospital - New York
California
- University of Southern California Keck School of Medicine - Los Angeles
Louisiana
- Louisiana State University School of Medicine - New Orleans
Missouri
- Washington University School of Medicine - St Louis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2024-06-10 |
| Est. Completion | 2030-07 |
| Phase | NA |
What NCT06444347 shows while recruiting
NCT06444347 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, below the 868-participant average among 9 other Hiatal Hernia trials with a reported enrollment target (77% lower).
The record links to 1 condition, with Hiatal Hernia appearing as the primary indexed condition, and to 2 interventions - of which Biosynthetic Mesh is the first listed.
NCT06444347 lists 6 locations in 4 states (New York, California, Louisiana).
Frequently Asked Questions
What is clinical trial NCT06444347 about?
NCT06444347 is a clinical study titled "Impact of Biosynthetic Mesh on Paraesophageal Hernia Repair". The aim of this study is to find out if using a certain kind of mesh can reduce the chances of hiatal hernias coming back after anti-reflux surgery. Participants undergoing antireflux surgery will be assigned to one of two groups, a group that has surgery with mesh, or a group that has surgery witho...
What is the current status of trial NCT06444347?
This trial is currently recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2024-06-10. Estimated completion is 2030-07.
What conditions does trial NCT06444347 study?
This clinical trial studies the following conditions: Hiatal Hernia.
What interventions are being tested in trial NCT06444347?
The interventions under investigation include: Biosynthetic Mesh (DEVICE), Hiatal Hernia Repair (PROCEDURE).
Who is sponsoring clinical trial NCT06444347?
This trial is sponsored by Weill Medical College of Cornell University, which has 701 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06444347 being conducted?
This trial has 6 study locations across California, Louisiana, Missouri, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Hiatal Hernia
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 NCT06444347's enrollment target sits among peer trials
200 2nd of 9 the highest of 9 other Hiatal Hernia trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Hiatal Hernia 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
-
Evaluating Clinical Hiatal Hernia Outcomes Using OviTex®
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-
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-
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ACTIVE NOT RECRUITING · NA
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Esophagogastric Junction Distensibility During Hiatal Hernia Repair
ACTIVE NOT RECRUITING · NA
-
Randomized EsophyX Versus Sham / Placebo Controlled TIF Trial: The RESPECT Study
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-
Miromatrix Biological Mesh for Hiatal Hernia Repair
COMPLETED · NA
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