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Analgesic Efficacy of Different Nerve Blocks in Postoperative Cesarean Section

Not Applicable
Recruiting
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
Inclusion Criteria
  • 18-40 years old
  • more or equal 37 weeks of gestation
  • ASA 1,2
  • Elective cesarean delivery
Exclusion Criteria
  • 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
GroupInterventionDescription
Intrathcal Morphine Groupintrathecal 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 groupintrathecal 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 groupintrathecal 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
NameTimeMethod
Duration of analgesia until first analgesic request.24 hours .

the time interval from immediate postoperative period until NRS reached 4

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Mahmoud Mamdouh Ekram

🇪🇬

Assiut, Manfalout, Egypt

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