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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02292043
Other study ID # wei liu
Secondary ID
Status Recruiting
Phase N/A
First received October 31, 2014
Last updated November 12, 2014
Start date May 2013
Est. completion date January 2015

Study information

Verified date November 2014
Source Harbin Medical University
Contact wei liu, Ph.D.
Phone 86-18904502999
Is FDA regulated No
Health authority China: Ministry of Health
Study type Observational

Clinical Trial Summary

The investigators would evaluate the effects of the novel method, HTEA on cardiac function in the heart failure patients secondary to idiopathic dilated cardiomyopathy and post-myocardial infarction.


Description:

The investigators would evaluate the effects of the novel method, HTEA on cardiac function in the heart failure patients secondary to idiopathic dilated cardiomyopathy and post-myocardial infarction. The specific index is 6 miniutes walk distance, echocardiography, NYHA, NTproBNP level, peripherial WBC, RBC, PLT, Cre, UA, K+, Na+ upon entrance to hospital and 4 weeks after HTEA treatment, and 3 months after discharge. The morbidity and re-hospitalization would also calculated 3 months after discharge.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date January 2015
Est. primary completion date January 2015
Accepts healthy volunteers No
Gender Both
Age group 20 Years to 80 Years
Eligibility Inclusion Criteria:

- 90 chronic cardiac failure patients in our hospital were selected and divided into two groups.

Exclusion Criteria:

- Vavular diseases

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Intervention

Drug:
HTEA
HTEA

Locations

Country Name City State
China Ren Xiaohui Harbin Heilongjiang
China the first affiliated hospital of Harbin Medical University Harbin Heilongjiang

Sponsors (1)

Lead Sponsor Collaborator
Harbin Medical University

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Morbidity 1 months to 3 months after discharge No
Secondary The decreased degree of NT-proBNP higher than 30% 3 months after discharge No
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