Clinical Trials Directory

Trials / Completed

CompletedNCT06232148

Cost Evaluation of Robotic Ventral Hernia Repair

Procedural Cost Analyses of Robotic Ventral Hernia Repair Compared With Laparoscopic or Open Repair: A Cohort Study

Status
Completed
Phase
Study type
Observational
Enrollment
3,000 (actual)
Sponsor
Bispebjerg Hospital · Academic / Other
Sex
All
Age
18 Years – 100 Years
Healthy volunteers

Summary

To evaluate the procedural cost of robotic ventral hernia repair compared with open ventral hernia repair.

Detailed description

Ventral hernia repair is one of the most frequently performed elective surgeries worldwide. The surgical approaches vary depending on the patient characteristics, type, and location the of ventral hernia, as well as the surgeons' preferences and equipment availability. The choice between an open or minimally invasive approach has been debated for years, and it seems clear that the risk of wound infection is significantly decreased when choosing a minimally invasive approach, whereas there are no significant difference in recurrence rates. In the past decades, the use of a robotic system for ventral hernia repair has gained increasing popularity due to an easy access to the preperitoneal or retromuscular plane with a minimally invasive technique. Two nationwide cohort studies concluded that length of stay and postoperative morbidity was decreased for robot-assisted repairs compared to open or laparoscopic ventral hernia repairs. Critics of robot-assisted surgery argue that it is time-consuming, too expensive, and that further cost-effectiveness analyses are needed to weigh the clinical benefits. The aim of these studies was to compare the procedure-specific cost of robot-assisted with open primary ventral and incisional hernia repair and thereafter with laparoscopic repairs.

Conditions

Interventions

TypeNameDescription
DEVICEType of surgery

Timeline

Start date
2017-01-01
Primary completion
2023-01-01
Completion
2023-05-01
First posted
2024-01-30
Last updated
2024-02-01

Source: ClinicalTrials.gov record NCT06232148. Inclusion in this directory is not an endorsement.