Status:
COMPLETED
Regional Analgesia After Cesarean Section
Lead Sponsor:
Medical University of Lublin
Conditions:
Cesarean Section
Pain, Postoperative
Eligibility:
FEMALE
18-75 years
Phase:
PHASE4
Brief Summary
All patients will be anaesthetized with spinal technique. Each patient will be treated with intravenous morphine - patient controlled analgesia (PCA). 2 of 3 groups of patients will receive ultrasound...
Detailed Description
Written consent will be obtained before the cesarean section. Only subarachnoidally anaesthetised patients may participate in the study. Pencil-point spinal needle and bupivacaine (Marcaine Heavy Spin...
Eligibility Criteria
Inclusion
- obtained consent
- singleton pregnancy
- subarachnoid anaesthesia
Exclusion
- coagulopathy
- allergy to morphine and local anesthetics
- depression, antidepressant drugs treatment
- epilepsy
- usage of painkiller before surgery
- addiction to alcohol or recreational drugs
Key Trial Info
Start Date :
September 4 2017
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 30 2019
Estimated Enrollment :
105 Patients enrolled
Trial Details
Trial ID
NCT03244540
Start Date
September 4 2017
End Date
August 30 2019
Last Update
February 18 2020
Active Locations (2)
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1
Szpital Specjalistyczny PRO-FAMILIA w Rzeszowie
Rzeszów, Poland, 35-001
2
Szpital Kliniczny Dzieciątka Jezus
Warsaw, Poland, 02-005