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Institutional Outcome Data From Per-oral Plication of the Esophagus

NCT03875365 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2024-04-11

No results posted yet for this study

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.

Conditions

  • Achalasia

Interventions

PROCEDURE

POPE

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

Sponsors & Collaborators

Principal Investigators

  • Shanda Blackmon · Mayo Clinic

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-10-02
Primary Completion
2024-01-19
Completion
2024-01-19

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03875365 on ClinicalTrials.gov