Enhancing Postoperative Pain Control in Laparoscopic Inguinal Hernia Surgery: Pre-peritoneal Bupivacaine Instillation with transversus abdominis plane block versus transversus abdominis plane block alone, a triple-blinded randomized controlled trial
Phase 3
Recruiting
- Conditions
- inguinal herniaPostoperative pain control, Laparoscopic inguinal hernia, Bupivacaine instillation, Transversus abdominis plane block, Randomized controlled trial
- Registration Number
- TCTR20240818001
- Lead Sponsor
- avamindrahiraj University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 70
Inclusion Criteria
1.Patients aged over 18 years.
2.Patients with unilateral inguinal hernia.
3.Patients scheduled for laparoscopic hernia surgery.
Exclusion Criteria
1.History of allergy to bupivacaine.
2.ASA (American Society of Anesthesiologists) classification IV-V.
3.Patients with bilateral inguinal hernia.
4.Patients who decline participation in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method