About this trial
Paraesophageal hernia can cause significant clinical symptoms, including reflux, chest pain, nausea, regurgitation, and even life threatening conditions such as bowel obstruction, and gastric volvulus. Repair of a paraesophageal hernia is associated with significant recurrence rate, with primary repair often in excess of 50%. Hernia recurrence and revisional surgery significantly increase the likelihood of complications and decreased quality of life.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
All patients age 18-80 undergoing elective or emergent paraesophageal hernia repair for symptomatic paraesophageal hernia will be eligible for enrollment into the study.
Disqualifiers
Patients with previous history of esophageal, gastric, diaphragmatic, or anti-reflux surgery will be excluded.
Trial population
Corewell Health General Surgery Patients
Trial design
Case-only
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Primary Outcome
Intraoperative Pre and Post hernia sac excision crural tension measurement will be collected.
Secondary outcomes
Competeness of hernia sac excision
Determining whether the hernia sac excision was complteted or partial
Paraesophageal hernia type
Comparing the paraesophageal hernia type
Mesh useage
Comparing the type of mesh used during the procedure
Complications
Following patients for post-op complications
Sponsors and contacts
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