Analgesic Efficacy of Different Nerve Blocks in Postoperative Cesarean Section
- Conditions
- Post Operative Pain
- Interventions
- Drug: intrathecal morphine for intrathecal morphine group . bupivacaine 0.25% for Quadratus Lumborum and Erector Spinae nerve block groups .
- Registration Number
- NCT06088420
- Lead Sponsor
- Assiut University
- Brief Summary
comparing analgesic efficacy of different nerve blocks on post operative cesarean sections.
- Detailed Description
Analgesic efficacy of Erector Spinae, Quadratus Lumborum and Intrathecal Morphine for post operative pain relief after cesarean section,
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Female
- Target Recruitment
- 120
- 18-40 years old
- more or equal 37 weeks of gestation
- ASA 1,2
- Elective cesarean delivery
- Patient refusal
- inability to cooperate with or understand the study
- local infection.
- bleeding disorder
- known anaphylaxis to any drug used in the trial
- ASA physical status more than 2
- emergency operations
- chronic opioid use (opioid use in the past 3 months)
- Neurologic deficit or disorder
- contraindication to regional anesthesia.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Intrathcal Morphine Group intrathecal morphine for intrathecal morphine group . bupivacaine 0.25% for Quadratus Lumborum and Erector Spinae nerve block groups . Intrathecal morphine administration for post operative pain relief after cesarean section Quadratus Lumborum nerve block group intrathecal morphine for intrathecal morphine group . bupivacaine 0.25% for Quadratus Lumborum and Erector Spinae nerve block groups . Quadratus Lumborum nerve block administration for post operative pain relief after cesarean section Erector Spinae nerve block group intrathecal morphine for intrathecal morphine group . bupivacaine 0.25% for Quadratus Lumborum and Erector Spinae nerve block groups . Erector Spinae nerve block administraion for post operative pain relief after cesarean section
- Primary Outcome Measures
Name Time Method Duration of analgesia until first analgesic request. 24 hours . the time interval from immediate postoperative period until NRS reached 4
- Secondary Outcome Measures
Name Time Method
Related Research Topics
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Trial Locations
- Locations (1)
Mahmoud Mamdouh Ekram
🇪🇬Assiut, Manfalout, Egypt