Clinical Trials Directory

Trials / Unknown

UnknownNCT01090219

Polypropylene Meshes in Hernia Repair

Morphofunctional Evaluations of Heavyweight and Ultralightweight Polypropylene Meshes in Men Inguinal Hernia Repair

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
32 (estimated)
Sponsor
Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude · Academic / Other
Sex
Male
Age
20 Years – 50 Years
Healthy volunteers
Not accepted

Summary

The aim of this study was to analyze the shrinkage of two different screens in the repair of inguinal hernias in men . 32 patients with unilateral inguinal hernia were assigned randomly. A Lichtenstein tension-free hernia repair was accomplished by emplacing heavy weight versus ultralight weight polypropylene meshes for repair of incisional hernia, marked next to the lips with six titanium clips (LT200).

Detailed description

eligibility criteria : Elective Surgery, men with unilateral inguinal hernia, 20 - 50 years Exclusion criteria: BMI\> 30, recurrent inguinal hernia, strangulated inguinal hernia, anesthetic risk ASA III and IV, Diabetics, COPD, benign prostatic hypertrophy,cancer disease outcome: Percentage of contraction of the different meshes by digital radiography in post-surgical days: 1, 30, 60 and 90 Independent variables: age, BMI, smoking, ethnicity, profession

Conditions

Interventions

TypeNameDescription
PROCEDUREtwo different meshes in the repair of inguinal herniasA Lichtenstein tension-free hernia repair was accomplished by emplacing Heavy-weight versus low-weight polypropylene meshes for repair of incisional hernia, marked next to the lips with six titanium clips (LT200)

Timeline

Start date
2008-02-01
Primary completion
2010-02-01
Completion
2010-07-01
First posted
2010-03-19
Last updated
2010-03-19

Locations

2 sites across 1 country: Brazil

Source: ClinicalTrials.gov record NCT01090219. Inclusion in this directory is not an endorsement.