Status:
COMPLETED
Comparison of the Quality of Recovery After Cesarean Section Surgery
Lead Sponsor:
Muğla Sıtkı Koçman University
Conditions:
Postoperative Recovery
Abdominal Pain
Eligibility:
FEMALE
18-45 years
Phase:
NA
Brief Summary
Inadequate pain control after cesarean section surgery causes postpartum depression, persistent pain and delayed mother-infant bonding. The investigator's aim is to asses whether ultrasound guided tra...
Eligibility Criteria
Inclusion
- American Society of Anesthesiologists physical status II-III
- Cesarean section surgery under spinal anesthesia
Exclusion
- American Society of Anesthesiologists physical status IV
- Emergency surgery
- General anesthesia
- Additional surgical intervention at the same session
- Body mass index of more than 35 kg/m2
- Allergy to any study drugs
- Local infection at the injection site
- History of drug abuse
- Communication problem
- Coagulopathy
- Preeclampsia and eclampsia
Key Trial Info
Start Date :
August 24 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 2 2023
Estimated Enrollment :
80 Patients enrolled
Trial Details
Trial ID
NCT05999981
Start Date
August 24 2023
End Date
November 2 2023
Last Update
November 13 2023
Active Locations (1)
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1
Mugla Sıtkı Kocman University Training and Research Hospital
Muğla, Turkey (Türkiye)