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Clinical trialNCT02211105TerminatedObservational

Registry to Compare Two Surgical Treatments for GERD

SponsorAmerican Gastroenterological AssociationEnrollment46GastroEsophageal Reflux Disease
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this prospective observational research study registry is to examine whether two GERD surgeries (Laparoscopic Nissen Fundoplication (LNF) or Transoral Incisionless Fundoplication (TIF)) have similar outcomes in effectiveness, safety, post-operative side effects and post-procedure costs associated with episodes of care and any ensuing complications.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

10 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Oc Reflux

    Huntington Beach, California, United States

  • Surgone Foregut Institute

    Englewood, Colorado, United States

  • Gi Solutions Inc

    Chicago, Illinois, United States

  • Northshore University Healthsystem

    Evanston, Illinois, United States

  • Lenox Hill Hospital

    New York, New York, United States

  • the Ohio State University Wexner Medical Center

    Columbus, Ohio, United States

  • Oregon Health & Science University

    Portland, Oregon, United States

  • University of Texas at Houston

    Bellaire, Texas, United States

  • Texas Tech University Health Sciences Center

    El Paso, Texas, United States

  • Reston Hospital Center/ Gw University

    Reston, Virginia, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Jul 2014
Primary completion
30 Apr 2017
Completion
30 Apr 2017
Last update posted
9 Jan 2018
Registered enrollment
46
Registry id
NCT02211105

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.