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Ultrasound-Guided TAP Block and Spinal Morphine for Pain Relief After Caesarean Section

Not Applicable
Completed
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
Inclusion Criteria
  • pregnant females scheduled for elective cesarean section
Exclusion Criteria
  • 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
GroupInterventionDescription
transversus abdominis plain block groupUltrasound-Guided Transversus Abdominis Plane Blockpost-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 groupMorphineintrathecal 150 microgram morphine in a 0.5 ml volume as an adjuvant to spinal anesthesia
Primary Outcome Measures
NameTimeMethod
prevention of post-operative pain72 hours

reduction of visual analogue scale post-operative

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Faculty of Medicine, Sohag University

🇪🇬

Sohag, Egypt

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