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TENS Use for Post-cesarean Pain Management

StatusNot Yet Recruiting
PhaseNot applicable
Started
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Record History

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  1. Start date: Aug 2026 to Sep 2026
    • Eligibility criteria expanded, about 14 words
    • Study description expanded, about 28 words
    • Publications: details revised at 18 of 18 entries
  2. Secondary endpoints: details revised at 1 of 15 entriesv2
  3. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
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.
Trial Details
NCT Number NCT07777939
Lead Sponsor Holy Family Hospital, Nazareth, Israel
Conditions
(from sponsor)		 Post Cesarean Pain Management
Enrollment 196 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov