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result of mesh fixation methods in groin hernia repairment

Phase 4
Conditions
inguinal hernia.
Inguinal hernia
Registration Number
IRCT20171213037857N3
Lead Sponsor
Babol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
120
Inclusion Criteria

patients aged 18 to 80 years
unilateral or bilateral inguinal hernia
patients with Liechtenstein Hernioplasty

Exclusion Criteria

known femoral hernia
large scrotal hernia
emergency operation for strangulated hernia
recurrent hernia
allergy to Bovin Aprotinin
patient refusal

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: Patient pain assessment was performed 7 days, one month and 6 months after Herniorrhaphy surgery. Method of measurement: Visual Analogue Scale.
Secondary Outcome Measures
NameTimeMethod
Recurrence of inguinal hernia. Timepoint: Evaluation of inguinal hernia recurrences was performed one month and 6 months after Herniorrhaphy surgery. Method of measurement: clinical examination.
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