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TAP Block vs LAWI for Analgesia Post-cesarean Section

Not Applicable
Completed
Conditions
Obstetric Pain
Obstetric Anesthesia Problems
Interventions
Procedure: Local anesthetic wound infiltration
Procedure: 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
Inclusion Criteria
  1. Women who underwent cesarean section under spinal anesthesia.
  2. Aged ≥19 years and less than 40 years.
  3. Gestational age ≥ 37 Weeks.
Exclusion Criteria
  1. Body mass index (BMI) ≥40 kg/m2.
  2. History of recent opioid exposure
  3. Hypersensitivity to any of the drugs used in the study.
  4. Significant cardiovascular, renal, or hepatic disease

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
LAWI groupLocal anesthetic wound infiltration40 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 groupTransversus Abdominis Plane BlockA 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
NameTimeMethod
degree of pain at rest and on movement (hip flexion and coughing) at 2, 4, 6, 12, and 24 hours postoperatively24 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
NameTimeMethod
measures the time to the first postoperative opioid dose24 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

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