● Recruiting

To Establish Whether Individuals With Premenstrual Dysphoric Disorder (PMDD) Demonstrate a Different Luteal-phase Sex Hormone Profile and Ratio Compared With Asymptomatic Controls.

Condition: Premenstrual Dysphoric Disorder ( PMDD) · Sponsor: Lancaster University

PhaseN/A

Planned participants50

Who can joinFemale, 18 Years to 45 Years

Healthy volunteersYes

About this study

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).

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

Talk to the study team

Milli Raizada, MBCHB Hons · +44 (0)1524 65201 · m.raizada2@lancaster.ac.uk

Always discuss trial participation with your own doctor first.

Locations (1)

Lancaster University

Lancaster, Lancashire, United Kingdom

Recruiting

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Source record: clinicaltrials.gov/study/NCT07686718