Analgesic Efficacy of Different Nerve Blocks in Postoperative Cesarean Section
Condition(s) studied
Investigational drug(s) / intervention(s)
Intrathcal Morphine Group: intrathecal morphine (150 μg) in addition to standard spinal anesthetic drugs(10-12 mg 0.5% hyperbaric bupivacaine)
Quadratus Lumborum nerve block(QL) group: intrathecal morphine (150 μg) in addition to standard spinal anesthetic drugs (10-12 mg 0.5% hyperbaric bupivacaine) + bilateral QL block by injecting 20 ml of 0.25% isobaric bupivacaine bolus with 4 mg ) dexamethasone as an adjuvant
Erector Spinae nerve block (ESP)group: intrathecal morphine (150 μg) in addition to standard spinal anesthetic drugs (10-12 mg 0.5% hyperbaric bupivacaine) + bilateral ESP block by injecting 20 ml of 0.25% isobaric bupivacaine bolus with 4 mg ) dexamethasone as an adjuvant
Study summary
comparing analgesic efficacy of different nerve blocks on post operative cesarean sections.
Eligibility
Primary outcome measure(s)
- Duration of analgesia until first analgesic request. — 24 hours .
the time interval from immediate postoperative period until NRS reached 4
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Mahmoud Mamdouh Ekram | Asyut | Manfalout | Recruiting |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06088420 on ClinicalTrials.gov ↗ ← All trials in Egypt