Clinical Trial

Post-operative Emesis and Pain Outcomes After Cesarean Delivery

Study acronym: EPOC
Active, Not Recruiting
View on ClinicalTrials.gov →
Summary
Approximately 20% women who undergo cesarean delivery would suffer from severe post-operative pain, which may further increase their risks from developing postpartum depression. Predictive factors such as pre-operative pain, age and anxiety could significantly contribute to post-operative nausea and vomiting (PONV) and pain in general surgery, however little information is available with regards to cesarean delivery. The investigators would investigate the risk factors of causing post-operative emesis after cesarean delivery, and to reaffirm that there is a positive correlation between pain on local anesthetic injection, presence of mechanical temporal summation (MTS) and post-Cesarean pain scores.
Protocol Amendment History 2 changes
notable Primary completion pushed: 2025-12-31 -> 2026-12-31 2026-08-08
minor Completion pushed: 2026-12-31 -> 2027-12-31 2026-08-08
Trial Details
NCT Number NCT03645239
Lead Sponsor KK Women's and Children's Hospital
Conditions Pain, Postoperative, Cesarean Section, Nausea, Postoperative, Vomiting, Postoperative
Enrollment 595 participants
Start Date 2018-05-24
Primary Completion 2026-12-31 (estimated)
Study Completion 2027-12-31 (estimated)
Updated on ClinicalTrials.gov 2026-08-07