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

Posted On: 2026-07-08

U.S., July 8 -- ClinicalTrials.gov registry received information related to the study (NCT07686718) titled 'To Establish Whether Individuals With Premenstrual Dysphoric Disorder (PMDD) Demonstrate a Different Luteal-phase Sex Hormone Profile and Ratio Compared With Asymptomatic Controls.' on June 22.

Brief 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).

Study Start Date: May 05

Study Type: OBSERVATIONAL

Condition: Premenstrual Dysphoric Disorder ( PMDD)

Recruitment Status: RECRUITING

Sponsor: Lancaster University

Information provided by (Responsible Party): Milli Raizada, Lancaster U...

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