Condition: Paraesophageal Hernia · GERD · Sponsor: David Krpata
The goal of this clinical trial is to compare whether the use of Ovitex mesh provides superior reduction in 2-year recurrence compared to pledgeted suture closure (no mesh) for patients undergoing paraesophageal hernia repair at the Cleveland Clinic. The main questions it aims to answer are: * Determine whether there is a difference in 2-year rates of radiographic recurrence with Ovitex versus pledgeted sutures in paraesophageal hernia repair. * Assess patient quality of life (QOL) after paraesophageal hernia repair with pledgets and mesh. A two-tailed research hypothesis will be used to determine whether there are differences between the two arms
This description comes directly from the study's public registry record.
David M Krpata, MD · 216 445-3441 · krpatad@ccf.org
William C Bennett, MD · 216 313-8971 · bennetw2@ccf.org
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| Cleveland Clinic Center for Abdominal Core Health | Cleveland, Ohio, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05974722