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CompletedNCT01504321

Polycystic Ovary Syndrome - Improving Outcomes

Polycystic Ovary Syndrome - Targeting the Sympathetic Nervous System to Improve Outcomes

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
42 (actual)
Sponsor
Baker Heart and Diabetes Institute · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Polycystic ovary syndrome affects a striking 9-18% of Australian reproductive aged women and has been associated with a number of metabolic abnormalities. Given the strong correlation between metabolic abnormalities and increased sympathetic activity, we hypothesise that reducing this activity using medication (moxonidine) can help improve the metabolic abnormalities, and therefore improve outcomes in polycystic ovary syndrome.

Conditions

Interventions

TypeNameDescription
DRUGMoxonidine0.2 mg/day moxonidine for 2 weeks 0.4 mg/day moxonidine for 3 months
DRUGPlaceboEncapsulated lactose powder

Timeline

Start date
2012-05-01
Primary completion
2015-05-01
Completion
2015-12-01
First posted
2012-01-05
Last updated
2018-11-02

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT01504321. Inclusion in this directory is not an endorsement.

Polycystic Ovary Syndrome - Improving Outcomes (NCT01504321) · Clinical Trials Directory