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Evaluation of Clinical Outcomes in Robotic-Assisted Inguinal Hernia Repair

NCT02684448 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 1258

Last updated 2017-03-28

No results posted yet for this study

Summary

This multi-center, retrospective data collection study will evaluate the feasibility, safety and performance of the da Vinci® surgical system for patients who have undergone robotic-assisted inguinal hernia repair, as well as provide information about the learning curve associated with robotic-assisted (da Vinci®) inguinal hernia repair.

In addition, this retrospective data collection study will evaluate the perioperative outcomes of robotic-assisted (da Vinci®) inguinal hernia repair and compare perioperative outcomes with those associated with open hernia repair by the same participating surgeon.

Conditions

  • Hernia, Inguinal
  • Hernia, Inguinal, Direct
  • Hernia, Inguinal, Indirect

Interventions

PROCEDURE

Inguinal Hernia Repair

Inguinal (unilateral or bilateral) hernia repair

Sponsors & Collaborators

  • Intuitive Surgical

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-01-31
Primary Completion
2016-06-30
Completion
2017-01-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02684448 on ClinicalTrials.gov