← Eichor
Study identifier: NCT07688720 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

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

Condition: Perimenopause · PMDD  ·  Sponsor: Texas Christian University

PhaseNA
Planned participants20
Who can joinFemale, 18 Years to 55 Years
Healthy volunteersNo

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.

This description comes directly from the study's public registry record.

Talk to the study team

Sarah E Hill, PhD  ·  817-257-6424  ·  s.e.hill@tcu.edu

Savannah A Hastings, M.S.  ·  817-257-4989  ·  s.a.hastings@tcu.edu

Always discuss trial participation with your own doctor first.

Locations (1)

Texas Christian UniversityFort Worth, Texas, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07688720