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Robotic Versus Hybrid Assisted Ventral Hernia Repair

NCT05233020 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2022-02-10

No results posted yet for this study

Summary

Laparoscopic ventral hernia repair (LVHR) may be associated with chronic pain, seroma formation, bulging and failure to restore abdominal wall function. These outcomes are risk factors for hernia recurrence and poor quality of life (QoL). Our study evaluates whether robotic-assisted ventral hernia repair (rVHR) diminish these complications compared to LVHR with primary closure of the defect (hybrid).

Conditions

  • Pain
  • Quality of Life
  • Recurrence

Interventions

DEVICE

robotic

fifteen patients undergo robotic operation

DEVICE

hybrid

fifteen patients undergo hybrid operation

Sponsors & Collaborators

  • Kuopio University Hospital

    lead OTHER

Principal Investigators

  • Pirjo Käkelä, PhD · gi -surgeon, clinical teacher

  • Pirjo Käkelä, PhD · gi-surgeon, clinical teacher

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-09-28
Primary Completion
2025-11-30
Completion
2025-11-30

Countries

  • Finland

Study Locations

More Related Trials

Entities

Diseases

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 NCT05233020 on ClinicalTrials.gov