NCT07896733|Recruiting
Anesthetic Technique and Quality of Recovery After Cesarean Delivery
Impact of Spinal, Epidural, and Combined Spinal Epidural Anesthesia on Quality of Recovery After Cesarean Delivery
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Impact of Spinal, Epidural, and Combined Spinal Epidural Anesthesia on Quality of Recovery After Cesarean Delivery
Sponsor study identifier
observational
180
1 country
1
Study Start
October 20, 2026
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Primary Completion
May 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
Study Completion
May 2, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
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.
Registry-reported information. Elapsed time and enrollment totals alone do not measure study progress or recruitment pace.
May 2, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
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Dates and qualifiers reported by the registry. Estimated dates do not confirm that a milestone has occurred.
October 20, 2026
Actual (reported)October 20, 2026
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
October 27, 2026
Actual (reported)May 1, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
May 2, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
ObsQoR score
The primary outcome will be the Obstetric Quality of Recovery score. The score will be assessed using the Obstetric Quality of Recovery questionnaire. Max score 110- min score 0
24 hours after cesarean delivery.
Rescue Analgesia
first 24 hours
Numeric rating scale (NRS)
first 24 hours
Cesarean section under spinal anesthesia
Cesarean section under epidural anesthesia
Cesarean section under combined spinal epidural anesthesia
Spinal anesthesia- 10-12 mg heavy marcaine+ 20 mcg fentanile depends on height
epidural catater placement- l3-l4. epidural bolus 15cc %0.5 bupivacaine 50mcg fentanil (total 16cc). after cs epidural pca was used.
These entries preserve how the registry describes the intervention. Their treatment roles are shown separately from molecular identities.
Administration procedure
Spinal anesthesia (heavy bupivacaine)
The registry describes an administration procedure or treatment schedule. Actual exposure and doses are not established by this entry.
View registry recordAdult women aged ≥18 years undergoing cesarean delivery under neuraxial anesthesia who provide written informed consent will be included. Participants will be categorized according to the anesthetic technique used: spinal, epidural, or combined spinal-epidural anesthesia.
Marmara University Pendik Training and Research Hospital
Istanbul, İ̇stanbul, Turkey (Türkiye)
First Submitted
October 20, 2026
First Posted
October 27, 2026
Study Start
October 20, 2026
Estimated (date passed)This estimate has passed. The registry has not confirmed an actual date for this milestone.
Primary Completion
May 1, 2027
Sensory Block Onset: Epidural vs Dural Puncture Epidural in Cesarean Section
l3-4 combine spinal epidural set was used. 10-12mg heavy marcaine 20 mcg fentanyl with spinal anesthesia. after cs epidural pca was used
Contact the study team to confirm eligibility.
Planned date reported by the registry; this milestone is not confirmed as achieved.
Study Completion
May 2, 2027
EstimatedPlanned date reported by the registry; this milestone is not confirmed as achieved.
Last Updated
October 27, 2026
Record last verified: 2026-10
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Source: ClinicalTrials.gov.
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