ClinicalTrials.gov record
Completed No phase listed Observational

A Prospective Study to Compare the Clinical Outcomes, Pain and Patient Quality of Life for Hernia Patients

ClinicalTrials.gov ID: NCT02715622

Public ClinicalTrials.gov record NCT02715622. 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 May 17, 2026, 7:31 AM EDT

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

Official title

A Prospective, Multicenter Post-Market Study to Evaluate and Compare the Clinical Outcomes, Pain and Patient Quality of Life After Open, Laparoscopic or Robotic Assisted Hernia (Incisional and Inguinal) Repair

Study identification

NCT ID
NCT02715622
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Intuitive Surgical
Industry
Enrollment
944 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 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
Mar 31, 2016
Primary completion
Sep 30, 2022
Completion
Sep 30, 2022
Last update posted
Feb 28, 2023

2016 – 2022

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Beverly Hills Hernia Center Beverly Hills California 90210
Vanderbilt University Medical Center Nashville California 37232
Kaiser Foundation Research Institute Oakland California 94612
Florida Hospital - Celebration Health Celebration Florida 34747
Baptist Health South Florida South Miami Florida 33143
Southern Illinois Healthcare Carbondale Illinois 62901
Rush University Medical Center Chicago Illinois 60612
Progressive Surgical Associates New Lenox Illinois 60451
Louisville Surgical Associates Louisville Kentucky 40215
Our Lady of the Lake Regional Medical Center Baton Rouge Louisiana 70808
Mercy Medical Center Baltimore Maryland 21202
Spectrum Health System Grand Rapids Michigan 49503
The Mount Sinai Medical Center New York New York 10029
New Hanover Regional Medical Center Wilmington North Carolina 28403
Hillcrest Medical Center Tulsa Oklahoma 74104
University of Tennessee Memphis Tennessee 38120
The Dallas VA Research Corporation Dallas Texas 75216

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 NCT02715622, 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 Feb 28, 2023 · Synced May 17, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02715622 live on ClinicalTrials.gov.

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