TTrialPathMatch Me to Trials
← Back to trials
RecruitingPerimenopausePMDD

Transcutaneous Auricular Neurostimulation (tAN) for Premenstrual Dysphoric Disorder (PMDD) and Perimenopause

Eligible age

18–55 yrs

Accepts

Women

Locations

1 state

Healthy volunteers

No

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

About this study

Transcutaneous Auricular Neurostimulation (tAN) will be administered to women with premenstrual syndrome (PMS), premenstrual dysphoric disorder (PMDD), and perimenopause. The investigators will examine whether tAN improves symptomology by collecting self-report data before the intervention, during the intervention, and following the intervention.

Sponsor: Texas Christian University

You may qualify if…

  • Assigned female at birth
  • Age 18 to 45
  • Naturally cycling
  • Regularly occurring menstrual cycle
  • Must identify as having PMS or PMDD
  • Reliable ability to complete online study surveys
  • Assigned female at birth.
  • Age 40 to 55

You may not qualify if…

  • Using hormonal birth control
  • Pregnant or lactating/breastfeeding
  • History of seizures
  • Implanted devices
  • Current or previous diagnosis of any heart conditions
  • Abnormal ear anatomy
  • Non-removable piercings on the ear
  • Recent ear infection

Where it's recruiting

Texas

Fort Worth

Source: ClinicalTrials.gov · NCT07688720 · last updated 2026-07-07

Transcutaneous Auricular Neurostimulation (tAN) for Premenstrual Dysph · TrialPath