NCT03875365

Institutional Outcome Data From Per-oral Plication of the Esophagus

Institutional Outcome Data From Per-oral Plication of the Esophagus (POPE)

• Status: Terminated
• Phase: —
• Study type: Observational
• Enrollment: 20 (actual)
• Sponsor: Mayo Clinic · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

Researchers are reviewing and analyzing surgical and clinical outcomes of subjects who underwent POPE for end-stage achalasia, a sigmoid esophagus, or a redundant conduit that has been used to replace the esophagus. This data will help researchers determine the safety and efficacy of a novel minimally invasive treatment compared to invasive surgery.

Detailed description

Researchers will be collecting electronic medical data for subjects who have already undergone Per-oral Plication of the Esophagus (POPE) procedure. Subject characteristics, radiographic documentation, videos, procedural details, and subject reported outcomes would be collected. This data will be used for review and analysis to answer questions aimed in this study. Data collected from this study will be entered into a database that will be maintained for future research.

Conditions

• Achalasia

Interventions

Type	Name	Description
PROCEDURE	POPE	Patients who have undergone Per-oral Plication of the Esophagus (POPE) procedure.

Timeline

• Start date: 2018-10-02
• Primary completion: 2024-01-19
• Completion: 2024-01-19
• First posted: 2019-03-14
• Last updated: 2024-04-11

Locations

3 sites across 1 country: United States