Viewing Study NCT02283450



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Study NCT ID: NCT02283450
Status: COMPLETED
Last Update Posted: 2014-11-05
First Post: 2014-11-02

Brief Title: Regulation of Immunological Cytokines by Qiliqiangxin Capsule in Dilated Cardiomyopathy Patients
Sponsor: Harbin Medical University
Organization: Harbin Medical University

Study Overview

Official Title: Regulation of Immunological Cytokines by Qiliqiangxin Capsule in Dilated Cardiomyopathy patients--a Randomized Double Blind Clinical Trial
Status: COMPLETED
Status Verified Date: 2014-11
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Purpose Research into the impact of Qiliqiangxin capsule on IFN-γIL-4NT-proBNP in dilated cardiomyopathy patients with heart failure

Methods Data were collected from the patients with idiopathic dilated cardiomyopathy cardiac function NYHA Ⅱ-Ⅳ in the first affiliated hospital of Harbin Medical University from May 2012 to April 2014 These 30 cases were treated under the recommendations of normal diagnosis and treatment in cardiomyopathy This experiment was randomized double-blindedthe experimental interferences were avoided and patients were divided into the experimental group and the placebo group The patients in experimental group received the relevant tests and inspections before the beginning of experimentsigned the informed consent Then the investigators get the venous blood centrifugalization and cryopreservation The patients take the medicine qiliqiangxin three times per dayfour tablets at a time Afrer a monththe investigators evaluated the symptomsthe function of heartblood pressureheart rate and keep blood specimens Three and six month laterelectrocardiogram and echocardiography were taken and the determination of the NT - proBNP was done The placebo group was followed up in the same way
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None