JRCT ID: jRCT2080220014
Registered date:01/09/2005
Basic Information
Recruitment status | |
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Health condition(s) or Problem(s) studied | Stable angina pectoris |
Date of first enrollment | 01/09/2005 |
Target sample size | |
Countries of recruitment | |
Study type | Interventional |
Intervention(s) | investigational material(s) Generic name etc : Nicorandil (SG-75) INN of investigational material : Therapeutic category code : 217 Vasodilators Dosage and Administration for Investigational material : SG-75 group: SG-75 5mg three times a day ISMN group: ISMN 20mg twice daily |
Outcome(s)
Primary Outcome | Efficacy: change in time to 1mm ST-segment depression in exercise tolerance test Safety: adverse drug reaction and adverse events |
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Secondary Outcome |
Key inclusion & exclusion criteria
Age minimum | >= 18age old |
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Age maximum | Not applicable |
Gender | Both |
Include criteria | 1)males or females older than 18 year-old 2)a history of stable angina pectoris for at least one month ( according to the Guideline for Diagnosis of Angina Pectoris in China) 3)chest pain being relievable by short-acting nitrates 4)willing to provid written informed consent |
Exclude criteria |
Related Information
Primary Sponsor | Chugai Pharmaceutical Co., Ltd. |
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Secondary Sponsor | |
Source(s) of Monetary Support | |
Secondary ID(s) | JapicCTI-050014 |
Contact
Public contact | |
Name | |
Address | Clinical-trials@chugai-pharm.co.jp |
Telephone | |
Affiliation | Chugai Pharmaceutical Co., Ltd., |
Scientific contact | |
Name | |
Address | |
Telephone | |
Affiliation |