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TENS for Postpartum Uterine Pain During Breastfeeding

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Minor Eligibility criteria expanded, about 11 words
    • Secondary endpoints: details revised at 1 of 6 entries
    • Publications: details revised at 6 of 6 entries
    • Study description shortened, about 1 word
  2. Notable Recruitment opened
    • Study sites: 1 to 2
    • Start date changed from estimate of Aug 1, 2026 to Aug 15, 2026
    v3
  3. Notable Start date: Jul 1, 2026 to Aug 1, 2026v2
  4. Minor 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  • Stopped: an ongoing trial was terminated, suspended or withdrawn.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.
This clinical study is designed to evaluate whether Transcutaneous Electrical Nerve Stimulation (TENS) is an effective, non-drug method to relieve postpartum uterine pain during breastfeeding in multiparous women (women who have given birth multiple times). Breastfeeding in the first 48 hours after delivery often triggers strong, painful uterine contractions due to the natural release of oxytocin. While standard care typically relies on pain-relief medications, this study investigates if TENS, a safe, low-cost device that sends gentle electrical impulses through small skin patches, can significantly reduce this pain and decrease the need for systemic medications. Participants will be randomly assigned to either receive standard postpartum pain medications or use a TENS device during two consecutive breastfeeding sessions. Researchers will measure and compare the peak pain levels between both groups using a standard 0 to 10 pain scale. The aim is examining whether TENS will significantly reduce postpartum uterine pain during breastfeeding and decrease medication use compared with standard care.
Trial Details
NCT Number NCT07703917
Lead Sponsor Holy Family Hospital, Nazareth, Israel
Conditions
(from sponsor)
Breast Feeding
Related terms Breast Feeding
Enrollment 124 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov