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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 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.

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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

FieldValue
Enrollment Target 200 participants
Start Date 2024-06-10
Est. Completion 2030-07
Phase NA

What the Registry Record Tells You About NCT06444347

The ClinicalTrials.gov registry entry for NCT06444347 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 868-participant average among 9 other Hiatal Hernia trials with a reported enrollment target (77% lower). The listed sponsor is Weill Medical College of Cornell University, which has 701 total studies on file at ClinicalTrials.gov.

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 reports 6 study locations spanning 4 distinct geographic areas - top geographies include 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.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.