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Clinical Trial Summary

The purpose of this study is to:

1. compare the long term results of mesh versus suture repair in treatment of abdominal wall defects;

2. find the optimal location of implanted prosthesis, comparing the two most useful position of mesh in abdominal wall hernia surgery.


Clinical Trial Description

To determine difference of operation time, applied materials of hernia operations; clinical complications, postoperative pain, hernia recurrence, recovery and normal activity time after surgery. ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Screening


Related Conditions & MeSH terms


NCT number NCT01018524
Study type Interventional
Source Hungarian Surgical Society
Contact
Status Completed
Phase Phase 4
Start date March 2002
Completion date March 2009

See also
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Completed NCT04435340 - Ventral Abdominal Hernia Repair With Self Adhering, Atraumatic Mesh N/A
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Completed NCT04947202 - Clinical Study on the Safety of SAFIL® MESH
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Completed NCT00245375 - A Trial Comparing Combination Therapy of Acetaminophen Plus Ibuprofen Versus Tylenol #3 for the Treatment of Pain After Outpatient Surgery N/A