Gastropexy in the Repair of Patients with Paraesophageal Hernias
Recruiting now · Not applicable
Conditions studied: Paraesophageal Hernia
In brief
Patients scheduled for surgery for primary paraesophageal herniation are randomized to either conventional surgical hernia repair or with the addition of gastropexy.
Key facts
- Study ID
- NCT06107634
- Run by
- Ersta Diakoni
- People needed
- 124
- Starts
- 2023-06-01
- Expected to finish
- 2030-08-02
- Last updated by the study team
- 2024-12-18
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients diagnosed with a primary paraesophageal hernia (hiatal hernia types II-IV) who are scheduled for elective or emergency surgical repair at participating centers
You may not qualify if…
- Previous major upper gastrointestinal (GI) surgery, including prior hiatal hernia repair.
- Diagnosis of achalasia or any other significant esophageal motility disorder.
- Inability to understand the purpose of the study and/or inability or unwillingness to provide informed consent.
- Severe comorbidities, defined by an American Society of Anesthesiologists (ASA) physical status score of greater than III.
Where it is running
- Sahlgrenska University Hospital — Gothenburg, Sweden (enrolling)
- Nyköping Hospital — Nyköping, Sweden (enrolling)
- Ersta Hospital — Stockholm, Sweden (enrolling)
- Sundsvall County Hospital — Sundsvall, Sweden (enrolling)
- Uppsala Academic Hospital — Uppsala, Sweden (enrolling)
- Skåne University Hospital Lund — Lund, Sweden
Full record on ClinicalTrials.gov
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