Trials / Completed
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
| Type | Name | Description |
|---|---|---|
| DRUG | Moxonidine | 0.2 mg/day moxonidine for 2 weeks 0.4 mg/day moxonidine for 3 months |
| DRUG | Placebo | Encapsulated 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.