Biologic Versus Synthetic Mesh for Treatment of Paraesophageal Hernia
Public ClinicalTrials.gov record NCT02242526. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
The investigators propose a randomized, single blinded controlled trial to compare the use of synthetic versus biologic mesh in hiatal hernia repair, two currently accepted standard of care surgical modalities. The investigators hypothesize that use of synthetic mesh will have lower recurrence at these time points compared to use of biologic mesh.
Study identification
- NCT ID
- NCT02242526
- Recruitment status
- Not listed
- Study type
- Interventional
- Phase
- Phase 4
- Enrollment
- 312 participants
Conditions and interventions
Conditions
Interventions
- Parietex™ Composite Hiatal Mesh, North Haven, CT Device
- Biodesign™ Surgisis® Graft, Cook Medical, Bloomington Device
Device
Eligibility (public fields only)
- Age range
- 18 Years to 80 Years
- Sex
- All
- Healthy volunteers
- Accepts healthy volunteers
This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.
Study timeline
- Start date
- Aug 31, 2014
- Primary completion
- Aug 31, 2019
- Completion
- Jul 31, 2020
- Last update posted
- Oct 14, 2018
2014 – 2020
United States locations
- U.S. sites
- 1
- U.S. states
- 1
- U.S. cities
- 1
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Stony Brook University Hospital | Stony Brook | New York | 11794 | Recruiting |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
Recently updated Hiatal Hernia trials
Other public records listing Hiatal Hernia. Sorted by last update posted; newest first. Not a recommendation.
- NCT07659080: Antireflux Surgery Without Preoperative Esophageal Manometry Not yet recruiting
- NCT00260585: Esophageal Cancer Risk Registry Recruiting
- NCT04450628: Esophagogastric Junction Distensibility During Hiatal Hernia Repair Active, not recruiting
- NCT07267494: Image-Guided Herniorrhaphy Study Not yet recruiting
- NCT07070115: Evaluating Clinical Hiatal Hernia Outcomes Using OviTex® Recruiting
- NCT06444347: Impact of Biosynthetic Mesh on Paraesophageal Hernia Repair Recruiting
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT02242526, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
- What this page does not do
- No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
- Where the data comes from
- Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
- Last refresh
- Last update posted Oct 14, 2018 · Synced Sep 8, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT02242526 live on ClinicalTrials.gov.