TAP Block vs LAWI for Analgesia Post-cesarean Section
- Conditions
- Obstetric PainObstetric Anesthesia Problems
- Interventions
- Procedure: Local anesthetic wound infiltrationProcedure: Transversus Abdominis Plane Block
- Registration Number
- NCT05447455
- Lead Sponsor
- Cairo University
- Brief Summary
Adequate pain control after cesarean delivery is a significant concern both for parturients and obstetric anesthesiologists. Transversus Abdominis Plane (TAP) block and local Wound infiltration with anesthetics are alternatives for reducing the severity of pain, total analgesic consumption, and opioid side effects. Both the TAP block and wound infiltration are superior to placebo; however, it is unknown which provides better analgesia after cesarean delivery because of a scarcity of randomized clinical trials. So, we hypothesized that the TAP block would decrease postoperative pain and postoperative cumulative opioid consumption at 24 hours
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 200
- Women who underwent cesarean section under spinal anesthesia.
- Aged ≥19 years and less than 40 years.
- Gestational age ≥ 37 Weeks.
- Body mass index (BMI) ≥40 kg/m2.
- History of recent opioid exposure
- Hypersensitivity to any of the drugs used in the study.
- Significant cardiovascular, renal, or hepatic disease
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description LAWI group Local anesthetic wound infiltration 40 mL of bupivacaine 0.25% was injected subcutaneously into the surgical wound (20 mL on each of the upper and lower sides) by the obstetrician before skin closure TAP block group Transversus Abdominis Plane Block A 22-gauge spinal needle was introduced from medial to lateral in-plane to the ultrasound probe, and 20 mL of bupivacaine 0.25% was injected under visualization in the plane between the transversus abdominis muscle and the fascia deep to the internal oblique muscle on each side.
- Primary Outcome Measures
Name Time Method degree of pain at rest and on movement (hip flexion and coughing) at 2, 4, 6, 12, and 24 hours postoperatively 24 hours , using a visual analog scale (VAS) score for pain intensity reported on 0-10-point scale for analysis. (0 = no pain and 10 = the worst possible pain).
- Secondary Outcome Measures
Name Time Method measures the time to the first postoperative opioid dose 24 hours cumulative opioid consumption at 2, 4, 6, and 12 hours. 12 hours
Trial Locations
- Locations (1)
faculty of medicine - Cairo university
🇪🇬Cairo, Kasr El Ainy, Egypt