RecruitingNCT07686718
To Establish Whether Individuals With Premenstrual Dysphoric Disorder (PMDD) Demonstrate a Different Luteal-phase Sex Hormone Profile and Ratio Compared With Asymptomatic Controls.
Sponsor
Lancaster University
Enrollment
50 participants
Start Date
May 5, 2026
Study Type
OBSERVATIONAL
Conditions
Summary
The aim of this project is to compare the ovarian hormone levels 7 days after ovulation and progesterone:oestradiol ratios between PMDD individuals and a control cohort (case control study).
Eligibility
Sex: FEMALEMin Age: 18 YearsMax Age: 45 Years
Plain Language Summary
Simplified for easier understanding
This clinical trial is studying a new treatment for people with premenstrual dysphoric disorder (pmdd). The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years to 45 Years.
This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.
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Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07686718