Ultrasound-Guided TAP Block and Spinal Morphine for Pain Relief After Caesarean Section
- Conditions
- Post Operative Pain
- Interventions
- Procedure: Ultrasound-Guided Transversus Abdominis Plane Block
- Registration Number
- NCT05331781
- Lead Sponsor
- Sohag University
- Brief Summary
This interventional double-blind randomized controlled study was carried out on 60 cases underwent elective caesarean section delivery, they were divided into 2 groups; patients were randomly allocated into two equal groups; Group M: received intrathecal 150 microgram morphine in a 0.5 ml volume, mixed with 10 mg of hyperbaric bupivacaine 0.5 % in a 2 ml volume (total volume 2.5 ml). Group B: received intrathecal 10 mg hyperbaric bupivacaine 0.5% 2ml volume + 0.5 saline (Total volume 3ml) and at the end of surgery patient received bilateral TAP block with 20 ml volume of 0.25% bupivacaine on each side.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 60
- pregnant females scheduled for elective cesarean section
- Patient refusal Patients with known allergies or with past history of allergy to local anesthesia Patients having an infection at the site of injection either in the back or in the abdominal region, Patients with coagulopathy or on systemic anticoagulation, Chronic opioid abuse, significant neurological, psychiatric or neuromuscular disease, Drug abuse and alcoholism, Obesity (BMI 30 and higher), Cardiovascular disease and Endocrine disorders.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description transversus abdominis plain block group Ultrasound-Guided Transversus Abdominis Plane Block post-cesarean section tap block will be given by ultrasound guidance using 20 ml bupivacaine local anesthetic 0.25% concentration for each side as an adjuvant to spinal anesthesia intrathecal morphia group Morphine intrathecal 150 microgram morphine in a 0.5 ml volume as an adjuvant to spinal anesthesia
- Primary Outcome Measures
Name Time Method prevention of post-operative pain 72 hours reduction of visual analogue scale post-operative
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Faculty of Medicine, Sohag University
🇪🇬Sohag, Egypt