TENS Use for Post-cesarean Pain Management
NCT: NCT07777939 · NOT_YET_RECRUITING
Brief Summary
The aim of this randomized controlled trial is to evaluate the effectiveness of continuous 24-hour Transcutaneous Electrical Nerve Stimulation (TENS) as an adjunct to standard postoperative care for pain management following cesarean delivery. Eligible women undergoing cesarean delivery under spinal anesthesia will be randomly assigned in a 1:1 ratio to either the intervention group, which will receive continuous TENS in addition to standard postoperative analgesia, or the control group, which will receive standard postoperative analgesia alone. The primary outcome is the Quality of Recovery-15 (QoR-15) score assessed 24 hours after cesarean delivery.
Frequently Asked Questions
What is TENS Use for Post-cesarean Pain Management?
TENS Use for Post-cesarean Pain Management is a clinical trial registered under NCT07777939. Current status: NOT_YET_RECRUITING.
What is the status of NCT07777939?
The current status of NCT07777939 (TENS Use for Post-cesarean Pain Management) is: NOT_YET_RECRUITING.
When did TENS Use for Post-cesarean Pain Management start?
TENS Use for Post-cesarean Pain Management started on 2026-08.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.