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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00212056
Other study ID # CSSCJ-1
Secondary ID UMIN_ID:C0000000
Status Completed
Phase N/A
First received September 13, 2005
Last updated October 31, 2007
Start date October 2001
Est. completion date December 2005

Study information

Verified date October 2007
Source National Cerebral and Cardiovascular Center
Contact n/a
Is FDA regulated No
Health authority Japan: Ministry of Health, Labor and Welfare
Study type Interventional

Clinical Trial Summary

To evaluate whether ANP as an adjunctive therapy for AMI reduces myocardial infarct size and improves regional wall motion.


Description:

The benefits of percutaneous coronary intervention (PCI) in acute myocardial infarction (AMI) are limited by reperfusion injury. In animal models, atrial natriuretic peptide (ANP) reduces infarct size, so the Japan-Working groups of acute myocardial Infarction for the reduction of Necrotic Damage by ANP(J-WINDANP) designed a prospective, randomized, multicenter study, to evaluate whether ANP as an adjunctive therapy for AMI reduces myocardial infarct size and improves regional wall motion.

Twenty hospitals in Japan will participate in the J-WIND-ANP study. Patients with AMI who are candidates for PCI are randomly allocated to receive either intravenous ANP or placebo administration. The primary end-points are (1) estimated infarct size (Σcreatine kinase and troponin T) and (2) left ventricular function (left ventriculograms). Single nucleotide polymorphisms (SNPs) that may be associated with the function of ANP and susceptibility of AMI will be examined. Furthermore, a data mining method will be used to design the optimal combinational therapy for post-MI patients.

J-WIND-ANP will provide important data on the effects of ANP as an adjunct to PCI for AMI and the SNPs information will open the field of tailor-made therapy. The optimal therapeutic drug combination will also be determined for post-MI patients.


Recruitment information / eligibility

Status Completed
Enrollment 600
Est. completion date December 2005
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 79 Years
Eligibility Inclusion Criteria:

1. Age 20-79 years

2. Chest pain of more than 30 min

3. 0.1 mV ST-segment elevation in 2 contiguous ECG leads

4. Admission to hospital within 12 h of symptom onset

5. First episode of AMI

6. Candidates for PCI

Exclusion Criteria:

1. History of old myocardial infarction

2. Left main coronary artery stenosis

3. Severe liver and/or kidney dysfunction

4. Suspected aortic dissection

5. History of coronary artery bypass graft

6. History of allergic response to drugs

7. Severe hypovolemia

8. Right ventricular infarction

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
ANP(hANP)
0·025 µg/kg per min for 3 days(intravenous)
Control
placebo

Locations

Country Name City State
Japan National Cardiovascular Center Suita Osaka

Sponsors (2)

Lead Sponsor Collaborator
National Cerebral and Cardiovascular Center Japan Cardiovascular Research Foundation

Country where clinical trial is conducted

Japan, 

References & Publications (1)

Minamino T, Jiyoong K, Asakura M, Shintani Y, Asanuma H, Kitakaze M; J-WIND Investigators. Rationale and design of a large-scale trial using nicorandil as an adjunct to percutaneous coronary intervention for ST-segment elevation acute myocardial infarction: Japan-Working groups of acute myocardial infarction for the reduction of Necrotic Damage by a K-ATP channel opener (J-WIND-KATP). Circ J. 2004 Feb;68(2):101-6. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary estimated infarct size 72hrs
Primary left ventricular function (left ventricular ejection fraction and end-diastolic volume) and regional wall motion 2-8weeks and 6-12months
Secondary survival rate 2.7years (median follow-up)
Secondary cardiovascular events (ie, cardiac death, nonfatal re-infarction, re-hospitalization because of cardiac disease, revascularization) 2.7years (median follow-up)
Secondary reperfusion injury (ie, malignant ventricular arrhythmia during reperfusion periods, re-elevation of ST-segment, worsening of chest pain) 24hrs
Secondary the association of SNPs of ANP-related genes with response to ANP treatment 2.7years (median follow-up)
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