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NCT02715622 · ClinicalTrials.gov registry record
A Prospective Study to Compare the Clinical Outcomes, Pain and Patient Quality of Life for Hernia Patients
A clinical trial of Inguinal Hernia and Hernia, sponsored by Intuitive Surgical.
- Completed
- Registry status
- 944
- Enrollment target
- 17
- Study locations
NCT02715622 is a study of Inguinal Hernia and Hernia that has completed, run by Intuitive Surgical. The registered enrollment target is 944 participants, above the 271-participant average among 11 other Inguinal Hernia trials with a reported enrollment target (248% higher). The trial reports 17 study locations across 12 states.
The verdict
NCT02715622, a study of Inguinal Hernia and Hernia, has completed, sponsored by Intuitive Surgical.
- COMPLETED
- Registry status
- 944 participants
- Enrollment target
- 17
- Study locations
Study Summary
The objective of this prospective, multi-center post-market study is to prospectively collect uniform, evidence based outcomes for patients undergoing open, laparoscopic or robotic assisted hernia repair. The outcomes that will be collected include various routine clinical parameters, short term patient reported outcomes (quality of life, pain scores) and long term hernia recurrence information. Patients will be treated according to standard of care at the surgeon's institution and patients will be followed up to collect information related to complications information and patient satisfaction associated with the hernia repair procedure.
Conditions Studied
Interventions
- PROCEDURE Hernia repair
Study Locations (17)
California
- Beverly Hills Hernia Center - Beverly Hills
- Vanderbilt University Medical Center - Nashville
- Kaiser Foundation Research Institute - Oakland
Illinois
- Southern Illinois Healthcare - Carbondale
- Rush University Medical Center - Chicago
- Progressive Surgical Associates - New Lenox
Florida
- Florida Hospital - Celebration Health - Celebration
- Baptist Health South Florida - South Miami
Kentucky
- Louisville Surgical Associates - Louisville
Louisiana
- Our Lady of the Lake Regional Medical Center - Baton Rouge
Maryland
- Mercy Medical Center - Baltimore
Michigan
- Spectrum Health System - Grand Rapids
New York
- The Mount Sinai Medical Center - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 944 participants |
| Start Date | 2016-04 |
| Est. Completion | 2022-10 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02715622
The ClinicalTrials.gov registry entry for NCT02715622 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 944 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 271-participant average among 11 other Inguinal Hernia trials with a reported enrollment target (248% higher). The listed sponsor is Intuitive Surgical, which has 40 total studies on file at ClinicalTrials.gov.
The record links to 5 conditions, with Inguinal Hernia appearing as the primary indexed condition, and to 1 intervention - of which Hernia repair is the first listed.
NCT02715622 reports 17 study locations spanning 12 distinct geographic areas - top geographies include California, Illinois, Florida.
Frequently Asked Questions
What is clinical trial NCT02715622 about?
NCT02715622 is a clinical study titled "A Prospective Study to Compare the Clinical Outcomes, Pain and Patient Quality of Life for Hernia Patients". The objective of this prospective, multi-center post-market study is to prospectively collect uniform, evidence based outcomes for patients undergoing open, laparoscopic or robotic assisted hernia repair. The outcomes that will be collected include various routine clinical parameters, short term pa...
What is the current status of trial NCT02715622?
This trial is currently completed. The enrollment target is 944 participants. The study started on 2016-04. Estimated completion is 2022-10.
What conditions does trial NCT02715622 study?
This clinical trial studies the following conditions: Inguinal Hernia, Hernia, Incisional Hernia, Hernia, Inguinal, Indirect, Hernia, Inguinal, Direct.
What interventions are being tested in trial NCT02715622?
The interventions under investigation include: Hernia repair (PROCEDURE).
Who is sponsoring clinical trial NCT02715622?
This trial is sponsored by Intuitive Surgical, which has 40 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02715622 being conducted?
This trial has 17 study locations across California, Florida, Illinois, Kentucky, Louisiana. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Inguinal Hernia
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Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.