CClinicalTrials.gg
CompletedNCT00212056Updated Nov 1, 2007

Japan-Working Groups of Acute Myocardial Infarction for the Reduction of Necrotic Damage by ANP

An interventional study of ANP(hANP) and Control in Acute Myocardial Infarction, sponsored by National Cerebral and Cardiovascular Center, Japan. Completed at 1 site in Japan. Open to participants aged 20 Years to 79 Years. Per ClinicalTrials.gov, last updated 2007-11-01.

Sponsored by National Cerebral and Cardiovascular Center, Japan · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
600
Allocation
Randomized
Ages
20 Years to 79 Years
Sex
All
01

Study summary

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

Read the detailed 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.

02

Conditions studied

  • Acute Myocardial Infarction

Keywords

  • Acute myocardial infarction
  • Atrial natriuretic peptide
  • Data mining
  • Randomized clinical trial
  • SNPs
03

In context

Myocardial Infarction

2,744 studies on the registry are indexed under Myocardial Infarction; 418 are open to participants now.

This study's planned enrollment of 600 is above the median of 148 across 1,595 interventional studies indexed under Myocardial Infarction.

Browse Myocardial Infarction studies →

Lead sponsor

National Cerebral and Cardiovascular Center, Japan is the lead sponsor of 19 studies on the registry; 3 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
20 Years to 79 Years
Sexes eligible
All
Accepts healthy volunteers
No

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

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
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
600 participants (estimated)

Study arms

  • Active comparator
    ANP

    Drug: ANP(hANP)

  • Placebo comparator
    Control

    Drug: Control

Interventions

  • DrugANP(hANP)

    0∙025 μg/kg per min for 3 days(intravenous)

  • DrugControl

    placebo

06

What researchers measure

Primary outcomes

  1. estimated infarct size

    Time frame: 72hrs

  2. left ventricular function (left ventricular ejection fraction and end-diastolic volume) and regional wall motion

    Time frame: 2-8weeks and 6-12months

Secondary outcomes

  1. survival rate

    Time frame: 2.7years (median follow-up)

  2. cardiovascular events (ie, cardiac death, nonfatal re-infarction, re-hospitalization because of cardiac disease, revascularization)

    Time frame: 2.7years (median follow-up)

  3. reperfusion injury (ie, malignant ventricular arrhythmia during reperfusion periods, re-elevation of ST-segment, worsening of chest pain)

    Time frame: 24hrs

  4. the association of SNPs of ANP-related genes with response to ANP treatment

    Time frame: 2.7years (median follow-up)

07

Study locations

1 site
  • National Cardiovascular Center
    Suita, Osaka 544-0024, Japan
08

References and documents

Publications

  • 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. doi: 10.1253/circj.68.101. PubMed 14745142 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 1, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00212056
Lead sponsor
National Cerebral and Cardiovascular Center, Japan
Collaborators
Japan Cardiovascular Research Foundation
First posted
Sep 21, 2005
Start date
Oct 2001
Completion
Dec 2005
Last update
Nov 1, 2007

Study contacts

Masafumi Kitakaze, MD, PhD
study chair · National Cerebral and Cardiovascular Center, Japan
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2007. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion