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Comparison between results of three different repair methods of unilateral inguinal hernia

Not Applicable
Recruiting
Conditions
nilateral inguinal hernia.
Unilateral inguinal hernia, without obstruction or gangrene
K40.9
Registration Number
IRCT20190511043548N1
Lead Sponsor
Arak University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Male
Target Recruitment
144
Inclusion Criteria

Men between age 18-75 years
Affected by unilateral inguinal hernia and without any complication
Having consent for participation in the study ( participants must be signed written consent form )

Exclusion Criteria

Affected by incarcerated hernia
Affected by recurrence hernia
Affected by bilateral hernia
MBI=35
Having concurrent abdominal surgery
Steroid therapy
Anti-platelet and anti-coagulant therapy
Having drug abuse history
Having liver cirrhosis
Hypersensitivity to Mesh or immune system deficiency

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Early postoperative complications (Acute pain, urinary retention, hematoma scrotal, hematoma ulcer, serum and wound infection). Timepoint: All patients in all three groups will undergo postoperative visit on the first day and the first week after surgery. Method of measurement: Observation and checklist- Pain will measure by 0–10 Numeric Pain Rating Scale.
Secondary Outcome Measures
NameTimeMethod
ate postoperative complications (Sensory disturbances, testicular atrophy, testicular pain, inguinal discomfort, pain during exertion, and relapse 9 months after surgery). Timepoint: 9 month after surgery. Method of measurement: Check list and observation- Pain will measure by 0–10 Numeric Pain Rating Scale.
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