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Transcutaneous Electrical Nerve Stimulation for Pain Mitigation During Intrauterine Device

Investigators are conducting a study to determine whether high frequency transcutaneous electrical nerve stimulation (hfTENS) is effective at reducing pain in women having an IUD inserted.

Condition(s)Pain
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryInvestigators are conducting a study to determine whether high frequency transcutaneous electrical nerve stimulation (hfTENS) is effective at reducing pain in women having an IUD inserted.
Who can participateInclusion Criteria: * Provision of signed and dated informed consent form for IUD Insertion * Stated willingness to comply with all study procedures * English speaking individuals aged 18 years or older * Presenting for IUD initiation during ambulatory care visit at MUSC Women's Health * Opting for either LNG 52mg or copper T380A IUD Exclusion Criteria: * Contraindication to IUD initiation (i.e. pregnancy, current pelvic infection, distorted uterine anatomy) * Contraindication or allergy to ibuprofen * History of a chronic pain disorder * Recent opioid use in the previous 30 days * History of a cardiac arrhythmia * History of heart disease (i.e. atrial fibrillation, congestive heart failure) * Presence of an implantable device with an electrical discharge (i.e. pacemaker) * BMI \> 50 (clas
Ages18 Years
SexFemale
Lead sponsorMedical University of South Carolina
LocationsCharleston, South Carolina, United States
Start date2025-12-01
NCT IDNCT06991075
Official listinghttps://clinicaltrials.gov/study/NCT06991075

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