EndoStim Patient Registry

NCT02441400 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 350

Last updated 2026-05-11

No results posted yet for this study

Summary

To provide a research tool enabling physicians to monitor long term clinical outcomes for patients undergoing gastroesophageal reflux disease (GERD) treatment with EndoStim LES Stimulation System.

Conditions

  • GERD

Interventions

DEVICE

EndoStim LES Stimulation System

Sponsors & Collaborators

  • EndoStim Inc.

    lead INDUSTRY

Principal Investigators

  • Virender K Sharma, MD · EndoStim Inc.

  • Joachim Labenz, MD · Diakonie Klinikum

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-31
Primary Completion
2022-07-12
Completion
2022-07-12

Countries

  • Argentina
  • Austria
  • Denmark
  • Germany
  • Mexico
  • Netherlands
  • United Kingdom

Study Locations

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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 NCT02441400 on ClinicalTrials.gov