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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01674686
Other study ID # 2011-12-069
Secondary ID
Status Recruiting
Phase Phase 4
First received August 24, 2012
Last updated February 7, 2018
Start date August 1, 2012
Est. completion date December 31, 2018

Study information

Verified date February 2018
Source Samsung Medical Center
Contact Hyeon-Cheol Gwon, MD,PhD
Phone 82-2-3410-3419
Email hcgwon@skku.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study was to to evaluate the effect of sarpogrelate, a selective serotonin receptor antagonist, and high dose statin on the reduction of coronary spasm in the patients with variant angina.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date December 31, 2018
Est. primary completion date December 31, 2018
Accepts healthy volunteers No
Gender All
Age group 20 Years to 70 Years
Eligibility Inclusion Criteria:

- Clinical history of chest pain compatible with variant angina; morning chest pain aggravated by cold exposure.

- Angiographically proven coronary spasm; TIMI flow < 3 by spontaneous coronary spasm or intracoronary ergonovine spasm provocation test.

Exclusion Criteria:

- Cardiac arrest by coronary spasm

- Left main coronary spasm

- Significant fixed coronary artery stenosis; Diameter stenosis > 70% in the major epicardial artery by coronary angiography

- Left ventricular ejection fraction < 30%

- Coagulation disorders or bleeding tendency (Platelet count < 50k, PT INR > 2.0)

- Significant liver disease (AST or ALT > 100 U/ml)

- Renal failure (S-Cr > 2.0 mg/dl)

- hypersensitivity for statin

- Pregnancy

Study Design


Intervention

Drug:
Sarpogrelate
Sarpogrelate 100mg twice a day
Atorvastatin
Atorvastatin 80mg daily

Locations

Country Name City State
Korea, Republic of Hyoen-Cheol Gwon, MD,PhD Seoul

Sponsors (1)

Lead Sponsor Collaborator
Samsung Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Ergonovine provocation test 12months later 1 year later
Secondary C-reactive protein lever 12months later 1 year
See also
  Status Clinical Trial Phase
Recruiting NCT03228238 - ANti-Oxidant in Variant Angina (ANOVA) Trial Phase 4
Completed NCT01444885 - Evaluate the Efficacy and Safety of Pletaal (Cilostazol) in Subjects With Vasospastic Angina Phase 2