Clinical Trials Directory

Trials / Completed

CompletedNCT01815957

Impact of Ranolazine on Coronary Microcirculatory Resistance

Impact of Ranalozine on Coronary Microcirculatory Resistance- A Prospective Single Center Study to Evaluate the Effect of Ranalozine in Microcirculatory Resistance (MICRO Study)

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
7 (actual)
Sponsor
University of New Mexico · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is being done to determine if Ranolazine treatment improves coronary microcirculation function among patients with coronary microcirculation dysfunction. We are also looking to learn if symptomatic improvement of chest pain during treatment with Ranalozine is related to improved coronary microcirculation function.

Conditions

Interventions

TypeNameDescription
DRUGRnalozine. After enrollment in the study, participants will initiate Ranolazine for 4 weeks. The participant's usual anti-anginal medication regimen will be continued unchanged throughout study duration. Patients will receive Ranolazine 500 mg orally twice daily for 1 week, and the dose will be increased to 1,000 mg twice daily for an additional 3 weeks if tolerated.

Timeline

Start date
2012-05-01
Primary completion
2016-03-01
Completion
2016-03-01
First posted
2013-03-21
Last updated
2023-12-26
Results posted
2023-12-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01815957. Inclusion in this directory is not an endorsement.