Comparison of Spinal Morphine and Transverse Abdominis Plane Block for Postoperative Pain Management in Patients Undergone Cesarean Section Under Spinal Anesthesia at Hawassa University Comphrensive and Specialized Hospital Ethiopia 2019: Randomized control trial
Phase 4
- Conditions
- SurgeryAnaesthesia
- Registration Number
- PACTR202002616299138
- Lead Sponsor
- Dilla University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
All ASA II
Age 18-45
Parturient who will undergo elective caesarean delivery
Pfannenstiel incision under spinal anaesthesia
Exclusion Criteria
•Patient refusal
•ASA 3 and above
•Caesarean delivery requiring epidural analgesia
•Preeclamptic
•Mothers with chronic pain disorder
•history of benzodiazepines taking
•history of opioid taking
•infection at needle insertion site
•coagulopathy disorder
•hypovolemic patient
• Allergy to local anaesthetics and morphine
•Failed spinal block or difficulty
•patients unable to self -report acute pain
•Cognitive impairment (Dementia, Alzheimer
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method •Time to first analgesic request in minutes<br>•Pain severity in NRS score<br>•Total postoperative Analgesia consumption in 24 hours<br>
- Secondary Outcome Measures
Name Time Method adverse effect of spinal Morphine