Status:
COMPLETED
Postoperative Analgesia in Cesarean Delivery
Lead Sponsor:
Gaziosmanpasa Research and Education Hospital
Conditions:
Postoperative Pain
Eligibility:
FEMALE
18-40 years
Phase:
NA
Brief Summary
İn this study, planned to compare the post-operative analgesic efficacy of Ilioinguinal iliohypogastric (II-IH) nerve block and Quadratus lumborum III Block in elective cesarean section operations. t...
Detailed Description
Patients who underwent elective cesarean section under spinal anesthesia will be divided into two groups at the end of the operation, using the closed envelope randomization method as Quadratus lumbor...
Eligibility Criteria
Inclusion
- Patients aged between 18 and 40
- ASA 2 risk group
- Patients at 37-41 weeks of pregnancy
- undergoing cesarean section under spinal anesthesia
Exclusion
- The patient does not accept the procedure.
- Patients with a history of eclampsia and preeclampsia during pregnancy
- local anesthetic allergy
- Infection at the procedure site
- Anticoagulant use with bleeding disorder
- Chronic analgesia and opioid use
- Mental, psychiatric and neurological problems
- Patients with ASA 3 and above with a history of any chronic disease.
Key Trial Info
Start Date :
May 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 1 2024
Estimated Enrollment :
70 Patients enrolled
Trial Details
Trial ID
NCT06010602
Start Date
May 1 2023
End Date
January 1 2024
Last Update
September 24 2024
Active Locations (1)
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1
Gaziosmanpasa Research and Education Hospital
Istanbul, Turkey (Türkiye), 34000