Overview

Evaluating The Quality of Recovery After Elective Cesarean Section

Status:
Recruiting
Trial end date:
2024-05-01
Target enrollment:
0
Participant gender:
Female
Summary
Adequately validated patient-reported outcome measures are available, which can assess recovery profiles following childbirth. This study will explore the effect of two different methods for pain management on the quality of recovery of pregnant women undergoing cesarean section
Phase:
N/A
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Ain Shams University
Criteria
Inclusion Criteria:

- American Society of Anesthesiologists physical status classification ΙΙ; and scheduled
for elective cesarean section using a low transverse Pfannenstiel incision with spinal
anesthesia.

Exclusion Criteria:

- (1) major hepatic, renal, or cardiovascular disease; (2) local infection; (3) bleeding
disorder; (4) any contraindication for spinal anesthesia; or (5) known allergy to any
drug used in the study (6) refusal to participate in the study (7) BMI > 35 (8) had
opioid dependence (9) chronic analgesic usage (10) inability to use patient controlled
analgesia (PCA) device.