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NCT07896733
Anesthetic Technique and Quality of Recovery After Cesarean Delivery
Conditions: Ceserean Section, Obstetric Quality of Recovery, Neuraxial Anesthesia
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: No
Enrollment: 180
Sponsor: Marmara University
Location: Marmara University Pendik Training and Research Hospital Istanbul İ̇stanbul
Summary
The goal of this prospective observational study is to evaluate whether the type of neuraxial anesthesia is associated with postoperative quality of recovery in adult women undergoing cesarean delivery. The main questions it aims to answer are:
Does postoperative Obstetric Quality of Recovery differ according to the neuraxial anesthetic technique used for cesarean delivery? Researchers will compare women receiving spinal anesthesia, epidural anesthesia, or combined spinal-epidural anesthesia to determine whether the anesthetic technique is associated with differences in postoperative quality of recovery.
Eligibility Criteria
Inclusion Criteria:
Age ≥18 years Undergoing cesarean delivery Willingness to participate in the study Providing written informed consent
Exclusion Criteria:
Contraindication to neuraxial anesthesia Conversion to general anesthesia Inability to understand or complete the Obstetric Quality of Recovery questionnaire Patients who are unable to breastfeed or hold their newborn due to the infant's admission to the neonatal intensive care unit after delivery Major intraoperative or postoperative complications that may independently affect recovery assessment Missing or incomplete 24-hour postoperative QoR assessment
Source: ClinicalTrials.gov (NCT07896733). StuddyBuddy aggregates publicly available trial information.