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Completed Phase 4 Interventional Results available

The CALIBER Study Randomized Controlled Trial of LINX Versus Double-Dose Proton Pump Inhibitor Therapy for Reflux Disease

ClinicalTrials.gov ID: NCT02505945

Public ClinicalTrials.gov record NCT02505945. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 2:29 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study compares mechanical sphincter augmentation (LINX Reflux Management System) to double-dose proton pump inhibitors (PPIs) for the management of reflux symptoms related to gastroesophageal reflux disease (GERD).

Study identification

NCT ID
NCT02505945
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Torax Medical Incorporated
Industry
Enrollment
152 participants

Conditions and interventions

Eligibility (public fields only)

Age range
21 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 2015 (Actual)
Primary completion
Oct 2017 (Actual)
Completion
Aug 2018 (Actual)
Last update posted
Jan 7, 2019

2015 – 2018

United States locations

U.S. sites
21
U.S. states
16
U.S. cities
21
Facility City State ZIP Site status
University of South Alabama Mobile Alabama 36617 —
Bapist Health Heber Springs Arkansas — —
University of Southern California Los Angeles California — —
UCSD San Diego California — —
SurgOne Foregut Institute Englewood Colorado 80110 —
Albany Surgical PC Albany Georgia — —
Esophageal Institute of Atlanta, PC. Atlanta Georgia 30309 —
St. Elizabeth Healthcare Edgewood Kentucky 41017 —
Anne Arundel Medical Center Annapolis Maryland — —
Cuyuna Regional Medical Center Crosby Minnesota 56441 —
Jersey Shore University Medical Center Neptune City New Jersey — —
Adirondack Surgical Group, LLC Saranac Lake New York — —
University Hospitals Cleveland Medical Center - Geauga Cleveland Ohio 44106 —
Knox Community Hospital Mount Vernon Ohio — —
The Oregon Clinic Portland Oregon — —
Albert Einstein Healthcare Network Philadelphia Pennsylvania 19141 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213 —
Scott and White Memorial Hospital Round Rock Texas 78665 —
Swedish Cancer Institute Seattle Washington — —
Gundersen Lutheran La Crosse Wisconsin — —
Medical College of Wisconsin Milwaukee Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02505945, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 7, 2019 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02505945 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →