Polycystic Ovary Syndrome Clinical Trial
Official title:
The Effect of Cipralex in Polycystic Ovary Syndrome
Objectives: To investigate the effect of Cipralex versus placebo on stress hormones, glucose
metabolism, physical and mental health and quality of life in polycystic ovary
syndrome(PCOS).
Treatment: 2x20 women for 12 weeks. Design: Double blinded, randomized, placebo controlled.
We want to investigate the effect of Cipralex versus placebo on stress hormones, glucose
metabolism, physical and mental health and quality of life in polycystic ovary
syndrome(PCOS).
PCOS is characterized by menstrual deregulation, high testosterone, mail hair growth and
increased stress hormones from the adrenals. Furthermore there are changes similar to those
seen in diabetes.
Cipralex is known to decrease stress hormones. But no investigations are on the effect of
cipralex on PCOS, or how the increased stress hormones affect the PCOS condition.
We will examine 2x20 women with PCOS. They will be randomized to Cipralex or placebo.
Treatment duration is 12 weeks.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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