Status:
NOT_YET_RECRUITING
Postoperative Recovery Quality After Cesarean Section: Comparing Erector Spinae and Retrolaminar Blocks Using Turkish Version of the Obstetric Quality-of-Recovery Score in a Turkish Cohort (ObsQoR-11T)
Lead Sponsor:
Elazıg Fethi Sekin Sehir Hastanesi
Conditions:
Postoperative Pain Management
Eligibility:
FEMALE
18-45 years
Brief Summary
Study Design This retrospective observational study aims to evaluate and compare the effects of two regional anesthesia techniques, Erector Spinae Plane (ESP) block and Retrolaminar Block (RLB), on po...
Detailed Description
METHODS 1.1. Study Design and Settings This was a retrospective, single-center observational study conducted to evaluate the effects of ESP and RLB on postoperative pain, opioid consumption, and pati...
Eligibility Criteria
Inclusion
- Inclusion Criteria
- Women aged 18-45 years, scheduled for elective cesarean delivery under spinal anesthesia.
- Gestational age ≥37 weeks, singleton pregnancy.
- Undergoing either ESP or RLB for postoperative analgesia.
- ASA Physical Status II-III.
- Ability to understand and complete ObsQoR-11T questionnaire.
- Provided written informed consent prior to participation. Exclusion Criteria
- Emergency cesarean delivery.
- Multiple pregnancy, preterm delivery (\<37 weeks),
- Severe maternal or obstetric complications (e.g., preeclampsia, placenta previa, placenta accreta spectrum), regardless of urgency.
- BMI ≥40 kg/m²
- Significant systemic diseases (e.g., severe cardiac, respiratory, renal, or hepatic disease).
- Fetal or placental anomalies.
- History of chronic pain syndromes, opioid dependence, or long-term analgesic use.
- Neurological, psychiatric, or cognitive disorders that may interfere with pain perception or questionnaire completion.
- Patients who declined participation or did not provide informed consent.
Exclusion
Key Trial Info
Start Date :
October 1 2025
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 15 2025
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT07181902
Start Date
October 1 2025
End Date
December 15 2025
Last Update
September 30 2025
Active Locations (1)
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1
Elazığ Fethi Sekin City Hospital
Elâzığ, Seçiniz, Turkey (Türkiye), 23100