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

StatusRecruiting
PhaseNot specified
Started
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Record History

  1. Study First Submitted
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).
Trial Details
NCT Number NCT07686718
Lead Sponsor Lancaster University
Conditions
(from sponsor)		 Premenstrual Dysphoric Disorder ( PMDD)
Related terms Premenstrual Dysphoric Disorder
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov