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Study identifier: NCT07070115 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Evaluating Clinical Hiatal Hernia Outcomes Using OviTex®

Condition: Hiatal Hernia  ·  Sponsor: Tela Bio Inc

PhaseNA
Planned participants173
Who can joinAll sexes, 22 Years to no upper limit
Healthy volunteersNo

About this study

This study will evaluate hiatal hernia recurrence rate and post-operative complications following the use of OviTex Core Resorbable or OviTex 1S Resorbable.

This description comes directly from the study's public registry record.

Talk to the study team

Melissa LaMantia, MA  ·  757-761-4922  ·  mlamantia@telabio.com

Danielle Campbell  ·  717-676-2589  ·  dcampbell@telabio.com

Always discuss trial participation with your own doctor first.

Locations (2)

University of South Alabama HealthMobile, Alabama, United StatesRecruiting
The University of Texas at Austin - Dell Medical SchoolAustin, Texas, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07070115