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Pain and Quality of Life After Retromuscular Ventral Hernia Repair (RECOVER)

NCT04487522 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 74

Last updated 2024-11-26

No results posted yet for this study

Summary

The study aims to explore the difference in outcomes relating to pain and quality of life after open, laparoscopic, and robotic-assisted retromuscular ventral hernia repair.

Conditions

  • Ventral Hernia

Interventions

PROCEDURE

Open retromuscular ventral hernia repair

With the subject under general anesthesia, a single incision is made in the abdomen. The retrorectus space is developed for mesh placement to repair the defect. The repair technique will be per the surgeon's standard of care.

PROCEDURE

Laparoscopic retromuscular ventral hernia repair

With the subject under general anesthesia, several small incisions are made in the abdomen. Ports are placed, the abdomen is insufflated, and laparoscopic instruments as well as a laparoscope are inserted to complete the repair. The retrorectus space is developed for mesh placement to repair the defect. The repair technique will be per the surgeon's standard of care.

DEVICE

Robotic-assisted retromuscular ventral hernia repair

With the patient under general anesthesia, several small incisions are made in the abdomen. Ports are placed, the abdomen is insufflated, and the da Vinci Robotic Surgical System (Intuitive) is docked to the subject and used to complete the procedure. The retrorectus space is developed for mesh placement to repair the defect. The repair technique will be per the surgeon's standard of care.

Sponsors & Collaborators

  • Intuitive Surgical

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
89 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-07-16
Primary Completion
2023-11-09
Completion
2024-09-19

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 NCT04487522 on ClinicalTrials.gov