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Evaluating the recurrence rate and adverse events of transversalis muscle fascia repair in total extraperitoneal repair (TEP) of inguinal hernia

Phase 2
Recruiting
Conditions
Inguinal hernia.
Inguinal hernia
Registration Number
IRCT20180312039067N2
Lead Sponsor
Esfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria

No history of abdominal surgery below the umbilical line
Primary direct hernia or unilateral or bilateral recurrent hernia
No history of mesh implantation
BMI less than or equal to 40
No history of liver disorder characterized by ascites
No history of renal failure
failure to complete written consent

Exclusion Criteria

Need to repair inguinal hernia with open surgery
Strangulated inguinal hernia

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Operation time. Timepoint: First randomization day. Method of measurement: STOPWATCH.;Hospitalization time. Timepoint: First randomization day. Method of measurement: Documentation in medical records.
Secondary Outcome Measures
NameTimeMethod
Recurrence. Timepoint: Post operation 7th day, 1st, 3rd and 6th months. Method of measurement: Clinical exam.;Pain. Timepoint: Post operation 7th day, 1st, 3rd and 6th months. Method of measurement: Visual Analogue Scale (VAS) measures pain intensity.;Seroma. Timepoint: Post operation 7th day, 1st, 3rd and 6th months. Method of measurement: Ultrasonography.;Infection. Timepoint: Post operation 7th day, 1st, 3rd and 6th months. Method of measurement: Clinical exam.;Analgesics. Timepoint: Post operation 7th day, 1st, 3rd and 6th months. Method of measurement: History taking.
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