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Polypropylene Meshes in Hernia Repair

U

Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude

Status

Unknown

Conditions

Inguinal Hernias

Treatments

Procedure: two different meshes in the repair of inguinal hernias

Study type

Interventional

Funder types

Other

Identifiers

NCT01090219
0002.0.379.174.08

Details and patient eligibility

About

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).

Full 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

Enrollment

32 estimated patients

Sex

Male

Ages

20 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elective Surgery
  • Men with unilateral inguinal hernia
  • Age 20 - 50 years

Exclusion criteria

  • BMI> 30
  • Recurrent inguinal hernia
  • Strangulated inguinal hernia
  • Anesthetic risk ASA III and IV
  • Diabetics
  • COPD
  • Benign prostatic hypertrophy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

32 participants in 1 patient group

two differents meshes
Experimental group
Description:
Heavy-weight versus low-weight polypropylene meshes
Treatment:
Procedure: two different meshes in the repair of inguinal hernias

Trial contacts and locations

2

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Central trial contact

Maria I Rosa, Ph.D.

Data sourced from clinicaltrials.gov

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