Premenstrual Dysphoric Disorder ( PMDD)

2

Review clinical trials related to Premenstrual Dysphoric Disorder ( PMDD). Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

The SPARK-PMDD Study

Scientists have found that the immune system, the body's system dedicated to fighting infections, can be in a state of "hyperactivity" (i.e., more active than you would normally expect) in some people with depression and postnatal depression, despite the lack of any actual ongoing infection. This response is referred to as inflammation. This discovery has unveiled unique opportunities to identify new medications to help patients with this heightened inflammation who have also not been responding to their antidepressant medications. This study aims to explore how inflammation in the body may be linked to symptoms of Premenstrual Dysphoric Disorder (PMDD) across the menstrual cycle, and how thoughts, emotions, and behaviours also may change throughout the cycle. We are recruiting two groups of people: People with a clinical or provisional (suspected) diagnosis of PMDD, and healthy controls who experience mild/no premenstrual changes. Over a two-month period, participants will complete daily psychological assessments across two menstrual cycles and will come into King's College Hospital (KCH) twice during one menstrual cycle to provide blood samples to measure their inflammation. By comparing these groups, we hope to gain a better understanding of the biological and psychological factors involved in PMDD, with the long-term goal of improving treatment options.

Participants needed: 120
Trial details
Age: 18-42Biological sex: FemaleType: ObservationalSponsor: King's College LondonUpdated: Aug 18, 2026Locations: 1
Eligibility criteria

Have been assigned female sex at birth (AFAB), with ovaries [+11]

Have a lifetime history of a psychotic disorder (including schizophrenia, schizo... [+10]

Status: Recruiting

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

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).

Participants needed: 50
Trial details
Age: 18-45Biological sex: FemaleType: ObservationalSponsor: Lancaster UniversityUpdated: Jul 7, 2026Locations: 1Duration: 6 Months
Eligibility criteria

Aged 18-45 years old (adults but less than the typical perimenopausal age so the... [+7]

Current use or use in the last 3 months of hormonal contraception such as the co... [+11]