Last updated: March 12, 2025
Sponsor: Istanbul Medipol University Hospital
Overall Status: Active - Recruiting
Phase
N/A
Condition
Hernia
Treatment
Port Site Infiltration
Transversalis Fascia Plane Block
Post Operative Pain Management
Clinical Study ID
NCT06778629
Medipol Hospital 5
Ages 18-65 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
American Society of Anesthesiologists (ASA) classification I- II Patients
Unilateral Inguinal Hernia Repair Surgery
Elective Operations
Exclusion
Exclusion Criteria:
Patients with a history of chronic pain
Evidence of infection in the intervention area
Allergy to local anesthetics
Coagulopathy
Body-mass index (BMI) ≥ 30
Body weight ≤ 50 kg
Patients who do not agree to participate in the study
Study Design
Total Participants: 60
Treatment Group(s): 3
Primary Treatment: Port Site Infiltration
Phase:
Study Start date:
February 14, 2025
Estimated Completion Date:
December 15, 2025
Study Description
Connect with a study center
Istanbul Medipol University Mega Hospital Complex
Istanbul, Bagcilar 34212
TurkeyActive - Recruiting
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