Clinical Trial

Premenstrual Syndrome Etiology Pilot Study

Study Description

Premenstrual Syndrome Etiology Pilot Study

PMSe is designed to evaluate reproductive and HPA axis hormone levels over the course of the menstrual cycle in women with Premenstrual Syndrome. Study objectives are to preliminarily show efficient kinetic modeling and absence of participant burden interfering with participant retention.

Location

Locations Selected Location

Methods

No pharmaceutical medication involved No pharmaceutical medication involved
Patients and healthy individuals accepted Patients and healthy individuals accepted

Procedure - Blood Draws

8 blood draws over one menstrual cycle

Additional Information

Official Study Title

Premenstrual Syndrome Etiology Pilot Study

Clinical Trial ID

NCT03862469

ParticipAid ID

e9rj8a