Study to Assess Efficacy of Nicorandil+Atenolol vs Atenolol in Treatment of Chronic Stable Angina.
Information source: Ferozsons Laboratories Ltd.
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Chronic Stable Angina
Intervention: Nicorandil (Drug); Atenolol (Drug)
Phase: Phase 4
Status: Recruiting
Sponsored by: Ferozsons Laboratories Ltd. Official(s) and/or principal investigator(s): Tariq Ashraf, MBBS,FCPS,FACC,FSCAI, Principal Investigator, Affiliation: National Institute of Cardiovascular Diseases
Overall contact: Tariq Ashraf, MBBS,FCPS,FACC,FSCAI, Phone: 092-03222999914, Email: tariqashraf2009@hotmail.com
Summary
This study is to determine the anti-anginal and anti-ischemic effect of k-channel opener,
nicorandil in patients of chronic stable angina.
Clinical Details
Official title: A Comparative Study to Assess the Efficacy of Nicorandil+Atenolol vs Atenolol in Treatment naïve Patients of Chronic Stable Angina.
Study design: Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: SPECT Tc99m- Tetrofosmin (MYOVIEW)
Secondary outcome: Exercise ECG Testing - Bruce protocol
Detailed description:
Stress myocardial perfusion imaging (MPI) is widely used for the diagnosis and risk
assessment of patients with known or suspected coronary artery disease (CAD). Also, MPI
lends itself to monitoring the effects of therapeutic interventions such as anti-ischemic
medications, gene therapy, and various percutaneous and surgical revascularization
modalities.
The effects of nitrates, potassium channel activators, calcium-channel blockers, and
beta-blockers on myocardial perfusion imaging are likely attributable to changes in
myocardial blood flow and myocardial oxygen supply-demand ratio. The major anti-ischemic
effect of BBs is a reduction in myocardial oxygen consumption both at rest and during
stress. Beta-blockers decrease myocardial oxygen demand through a reduction in heart rate,
blood pressure, and myocardial contractility. They also prolong diastole, therefore
increasing coronary perfusion time. The effect of chronic atenolol use on dipyridamole SPECT
MPI was assessed in a randomized, double-blind, crossover study that showed no difference in
the perfusion defect size and severity between placebo and atenolol for the group as a
whole, although one-third of patients had larger defects on atenolol than placebo. Bridges
et al., 1992 (56)
Nicorandil, a potassium channel activator, when given for 3 weeks exhibited significant
improvement in myocardial perfusion in both MI and angina patients, on exercise thallium
scan. Yamazaki et al., 1993 (69).
Atenolol as shown in the cross over study does not affect myocardial perfusion significantly
and hence combination therapy with nicorandil will help us to determine a significant
benefit of nicorandil on MP. Results will be analyzed from base line in the same arm and the
difference will be further compared with control arm.
Guidelines suggest beta blockers as first line of therapy. To assess the anti ischemic
effects of nicorandil, combination therapy with atenolol will be compared with atenolol
alone. Since atenolol effect on MP is insignificant an added advantage of nicorandil can be
evaluated in comparative study.
Primary objective is to assess the anti ischemic effect of nicorandil.
The primary endpoint is to compare the anti ischemic effect over 4 weeks period.
Changes in perfusion will be evaluated in each arm at week 4 and comparison between the two
study arms will be made to document the anti ischemic effects of nicorandil.
Primary efficacy variables of the study are the difference of the following endpoints from
the baseline at week 4 and comparison between control and study arm using Ex- SPECT MPI.
Secondary efficacy variables of the study are the difference of the following endpoints from
the baseline and comparison between control and study arm using ETT Bruce Protocol at week
4.
Secondary objectives of the study are to evaluate the anti anginal effect and safety of
Nicorandil.
This is an open label, randomized controlled pilot study. Sponsor of this study is Ferozsons
Labs. Ltd. All participating patients must sign a written informed consent form.
Eligible patients with proven CAD having at least one reversible or partially reversible
myocardial perfusion defects on MPI SPECT - Tc-99m and functional class I & II of CSA, and
laboratory values within predefined safety limits will be recruited.
Chief exclusion criteria include presence of only fixed perfusion defects, CSA functional
class III and IV and prior revascularization.
A total of 40 patients will be enrolled in the study, 20 patients in each arm). Patients
will be randomized in a 1: 1 fashion to receive beta blocker in combination with nicorandil
(experiment arm) or beta blocker (control arm) for four weeks until unacceptable toxicity,
withdrawal of consent, whichever comes first.
Nicorandil dose will be titrated from 10mg bd for 7days to 20mg bd for next 3 weeks.
Concurrent therapy for angina attacks will be allowed to be used with study medication.
All patients will have treadmill exercise using Bruce protocol. At peak exercise, 10-15 mCi
of technetium - 99m tetrofosmin is injected and patient will exercise an additional 1 to 2
minutes.. Stress SPECT images will be acquired beginning 15 to 45 minutes after the
completion of treadmill stress. At rest 30 mCi of technetium-99m tetrofosmin will be
injected and SPECT images will be acquired using same protocol.
Study monitoring at the centre will be provided by the sponsor
Eligibility
Minimum age: 25 Years.
Maximum age: 65 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
1. Patients of chronic stable angina with abnormal Exercise Myocardial Perfusion Spect
Scan with reversible and partially reversible ischemic changes.
2. Male and female
3. Age 25 to 65 years
4. Patient must understand and be willing, able and likely to comply with all study
procedures and restrictions and comprehends the diary cards.
5. Patient must be able to give voluntary written informed consent.
Exclusion Criteria:
1. Hypertension of > 170/100 mm of Hg
2. Valvular heart disease and cardiomyopathy
3. Myocardial infarction in < 6 months
4. Unstable angina
5. Congestive cardiac failure
6. Severe anemia (Hb 7G/dl)
7. Cardiac arrhythmias or II or III degree AV block
8. Significant liver or renal dysfunction
9. IDDM (Type-1 diabetes mellitus)
10. Systolic blood pressure < 100 mm Hg
11. Pregnant and nursing women
12. Known hypersensitivity to nicorandil
13. On calcium channel blockers
14. Patients not eligible for Tc 99m SPECT
15. Patients in whom beta blockers are contraindicated
16. Geographical inaccessibility for treatment or follow-up evaluations
Locations and Contacts
Tariq Ashraf, MBBS,FCPS,FACC,FSCAI, Phone: 092-03222999914, Email: tariqashraf2009@hotmail.com
National Institute of Cardiovascular Diseases, Karachi, Sind 75850, Pakistan; Recruiting Tariq Ashraf, MBBS, FCPS, FACC, FSCAI, Phone: 092-03222999914, Email: tariqashraf2009@hotmail.com Hamid Tirmizey, MBBS, BSC, DIP. CARD, Phone: 092-03212215383, Email: alafzal1@yahoo.com Tariq Ashraf, MBBS, FCPS, FACC, FSCAI, Principal Investigator
Additional Information
Starting date: September 2011
Last updated: December 7, 2011
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