NIPH Clinical Trials Search

UMIN ID: UMIN000001763

Registered date:10/03/2009

Randomised open-label compatrison study between carperitide and non-carperitide therapy for acute decompensated heart failure

Basic Information

Recruitment status Pending
Health condition(s) or Problem(s) studiedAcute decompensated heart failure
Date of first enrollment2009/01/01
Target sample size200
Countries of recruitmentJapan
Study typeInterventional
Intervention(s)more than two days administration of carperitide more than two days administration of intra-venous heart failure treatment drug


Primary OutcomeEvaluation of cchangingthe concentration of serum creatinine, estimated GFR and BUN within 7 days after administration of intravenous heart failure agents (carperitide or niterates)
Secondary Outcome

Key inclusion & exclusion criteria

Age minimum20years-old
Age maximumNot applicable
GenderMale and Female
Include criteria
Exclude criteria1) eGFR<15ml/min/1.73m or hemodialysis 2) Severe hypotention or cardioganic shock 3) Patients with dehydration 4) Dominant rightventricular heart failure 5) Intubated patients 6) Acute myocardial infarction 7) Patients with cancer 8) Patients with pregnancy 9) Prior enrollment

Related Information


public contact
Name Shinichi Shirai
Address Japan
Affiliation Kokura Memorial Hospital Cardiology
scientific contact
Name Masashi Iwabuchi
Address 1-1 Kifunemachi Kokurakita-ward Kitakyushu Japan
Affiliation Kokura Memorial Hospital Cardiology