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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01562041
Other study ID # CPJMR0032105
Secondary ID
Status Terminated
Phase Phase 2
First received
Last updated
Start date March 9, 2012
Est. completion date January 2, 2014

Study information

Verified date May 2021
Source Novartis
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study was designed to evaluate the use of ETT electrocardiogram (ECG) indices as biomarkers in the assessment of atherosclerotic coronary vascular disease (ASCVD).


Recruitment information / eligibility

Status Terminated
Enrollment 14
Est. completion date January 2, 2014
Est. primary completion date January 2, 2014
Accepts healthy volunteers No
Gender All
Age group 40 Years to 75 Years
Eligibility Inclusion Criteria: - History of stable coronary artery disease Exclusion Criteria: - Inability or unwillingness to participate in multiple exercise treadmill tests and/or any other requirements of this study as assessed by the Investigator. - History of chronic atrial fibrillation. Other protocol-defined inclusion/exclusion criteria may apply.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Ranolazine 500 mg
Ranolazine 500 mg, oral tablet, b.i.d.

Locations

Country Name City State
United States Novartis Investigative Site Jacksonville Florida
United States Novartis Investigative Site New York New York

Sponsors (1)

Lead Sponsor Collaborator
Novartis Pharmaceuticals

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change From Baseline in Maximum ST Segment Change Adjusted for Heart Rate (ST-HR) Index ST/HR index was measured as the average change in ST segment depression relative to heart rate change over the entire duration of exercise, monitored by ECG during the exercise treadmill tests. Change in maximum ST/HR index between the average of tests 1-3 (pre Ranexa® treatment) performed during baseline period and test 4 (post Ranexa® treatment) during treatment period was reported. Baseline up to Day 15
Primary Change From Baseline in Maximum ST Segment Change Adjusted for Heart Rate (ST-HR) Slope ST-HR slope is an index of exercise induced ischemia. Linear regression was used to determine the slope of the ST/HR relationship in a participant's ECG response monitored during the exercise treadmill test. The highest ST segment/heart rate slope from among all the ECG leads and the X-axis intercept of the associated line were used to generate the maximum slope. Change in maximum ST-HR slope between the average of tests 1-3 (pre Ranexa® treatment) performed during baseline period and test 4 (post Ranexa® treatment) during treatment period was reported. Baseline up to Day 15
Primary Change From Baseline in X-Axis Intercept of ST-HR Slope Linear regression was used to determine the slope of the ST/HR relationship in a participant's ECG response monitored during the exercise treadmill test. Change in X- axis intercept of ST-HR slope between the average of tests 1-3 (pre Ranexa® treatment) performed during baseline period and test 4 (post Ranexa® treatment) during treatment period was reported. Baseline up to Day 15
Secondary Change From Baseline in Total Exercise Duration Total exercise duration was defined as the elapsed time between the start of exercise and termination of exercise for severe angina, dyspnea or extreme fatigue assessed during the exercise treadmill test. Change in the duration of exercise between the average of tests 1-3 (pre Ranexa® treatment) performed during baseline period and test 4 (post Ranexa® treatment) during treatment period was reported. Baseline up to Day 15
Secondary Change From Baseline in Time to Onset of 1 mm ST Segment Depression (Time to Ischemia) Exercise-induced ischemia was defined as the new development of horizontal or down sloping ST-segment depression (= 1 mm at 60 milliseconds after the J point) vs. baseline tracings. Change in time to onset of 1 mm ST depression between the average of tests 1-3 (pre Ranexa® treatment) performed during baseline period and test 4 (post Ranexa® treatment) during treatment period was reported. Baseline up to Day 15
Secondary Change From Baseline in Time to Onset of Angina Time to onset of angina was defined as the elapsed time between the start of exercise and the onset of anginal chest pain as reported by the participant. Change in time to angina between the average of tests 1-3 (pre Ranexa® treatment) performed during baseline period and test 4 (post Ranexa® treatment) during treatment period was reported. Baseline up to Day 15