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NCT03735862 · ClinicalTrials.gov registry record
Complications, Outcomes and Revisions Following Hiatal Hernia Repair With MIROMESH
A clinical trial of Gastroesophageal Reflux and GERD, sponsored by Miromatrix Medical.
- Completed
- Registry status
- 85
- Enrollment target
- 1
- Study location
NCT03735862 is a study of Gastroesophageal Reflux and GERD that has completed, run by Miromatrix Medical. The registered enrollment target is 85 participants, below the 182-participant average among 25 other Gastroesophageal Reflux trials with a reported enrollment target (53% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03735862, a study of Gastroesophageal Reflux and GERD, has completed, sponsored by Miromatrix Medical.
- COMPLETED
- Registry status
- 85 participants
- Enrollment target
- 1
- Study location
Study Summary
Investigator will identify a consecutive cohort of patients who have undergone a hiatal hernia repair and are at least 6 months post index procedure.
Conditions Studied
Interventions
- BIOLOGICAL Hepatic derived surgical matrix
Study Locations (1)
Virginia
- Virginia Heartburn and Hernia Institute - Lorton
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 85 participants |
| Start Date | 2017-06-01 |
| Est. Completion | 2018-10-01 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03735862
The ClinicalTrials.gov registry entry for NCT03735862 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 85 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 182-participant average among 25 other Gastroesophageal Reflux trials with a reported enrollment target (53% lower). The listed sponsor is Miromatrix Medical, which has 4 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Gastroesophageal Reflux appearing as the primary indexed condition, and to 1 intervention - of which Hepatic derived surgical matrix is the first listed.
NCT03735862 reports 1 study location spanning 1 distinct geographic area - top geographies include Virginia.
Frequently Asked Questions
What is clinical trial NCT03735862 about?
NCT03735862 is a clinical study titled "Complications, Outcomes and Revisions Following Hiatal Hernia Repair With MIROMESH". Investigator will identify a consecutive cohort of patients who have undergone a hiatal hernia repair and are at least 6 months post index procedure.
What is the current status of trial NCT03735862?
This trial is currently completed. The enrollment target is 85 participants. The study started on 2017-06-01. Estimated completion is 2018-10-01.
What conditions does trial NCT03735862 study?
This clinical trial studies the following conditions: Gastroesophageal Reflux, GERD, Hiatal Hernia With Gastroesophageal Reflux Disease.
What interventions are being tested in trial NCT03735862?
The interventions under investigation include: Hepatic derived surgical matrix (BIOLOGICAL).
Who is sponsoring clinical trial NCT03735862?
This trial is sponsored by Miromatrix Medical, which has 4 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03735862 being conducted?
This trial has 1 study location across Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Read our methodology - how this data is sourced, computed, and verified.
Related
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