A Prospective Study to Compare the Clinical Outcomes, Pain and Patient Quality of Life for Hernia Patients
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.
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
Conditions
Interventions
- Hernia repair Procedure
Procedure
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.