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Clinical Trials/NCT01953302
NCT01953302CompletedNot Applicable

Modified "Open Intraperitoneal Mesh" Technique of Incisional Ventral Hernia Repair

Varazdin General Hospital2 sites in 1 country124 target enrollmentStarted: May 1, 2010Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
124
Locations
2
Primary Endpoint
Number of Early Postoperative Complications (Wound Infections, Seroma, Hematoma)

Study Overview

Brief Summary

Ventral hernias, primary and recurrent, are major surgical challenge. We aim to investigate efficacy of modified technique of ventral hernias repair: an "open intraperitoneal mesh" technique.

Detailed Description

We analyzed early postoperative complications (EPCs; wound infection, hematoma, and seroma) and late postoperative complications (recurrence) in 124 patients operated for IHs and recurrent IHs (RIHs) using our new technique. Our technique involved repairing hernias by preserving the hernia sac, which was later used to conceal the mesh that replaced the abdominal wall defect, thus dividing the mesh from subcutaneous tissue.

Study Design

Study Type
Interventional
Allocation
Na
Intervention Model
Single Group
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • patients aged 18 years or older
  • American Society of Anesthesiologists physical status I, II, III

Exclusion Criteria

  • refusal of the patients to give informed consent

Outcomes

Primary Outcomes

Number of Early Postoperative Complications (Wound Infections, Seroma, Hematoma)

Time Frame: four weeks after the surgery

we counted number of patinetns with wound infection, seroma, hematoma that occured in the early postoperative time

Secondary Outcomes

  • Number of Patients With Postoperative Hernia Recurrence(up to 36 months after the surgery)

Investigators

Sponsor
Varazdin General Hospital
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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