Trials / Completed
CompletedNCT02252406
Impact of Ranolazine in Blood Markers in Women With Angina and Metabolic Syndrome
Impact of Ranolazine on Inflammatory, Thrombogenic, Lipogenic, Biomarkers in Women With Angina and Metabolic Syndrome.
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 33 (actual)
- Sponsor
- University of Florida · Academic / Other
- Sex
- Female
- Age
- 30 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the effects of ranolazine on different markers of cardiometabolic disease in women with stable angina.
Detailed description
Evaluate the ability of ranolazine to favorably modify thrombogenic, inflammatory, lipogenic, oxidative stress and hormonal biomarkers in a relatively short period of time in a group of ethnically diverse women with chronic stable angina and metabolic syndrome.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Ranolazine | Ranolazine 500 mg from baseline to week 3 and 1000 mg thereafter until week 24 |
| OTHER | Placebo | Matching placebo tablets daily for 24 weeks. |
Timeline
- Start date
- 2015-09-01
- Primary completion
- 2018-12-17
- Completion
- 2019-05-17
- First posted
- 2014-09-30
- Last updated
- 2020-04-10
- Results posted
- 2020-04-10
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT02252406. Inclusion in this directory is not an endorsement.