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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00453752
Other study ID # KB/66/2006
Secondary ID
Status Recruiting
Phase N/A
First received March 28, 2007
Last updated March 28, 2007
Start date April 2006
Est. completion date April 2010

Study information

Verified date March 2006
Source Medical University of Warsaw
Contact Ciurzynski Michal, M.D, Ph.D
Phone +48 22 502 11 44
Email mciurzyn@amwaw.edu.pl
Is FDA regulated No
Health authority Poland: Ministry of Health
Study type Observational

Clinical Trial Summary

The aim of this study was to assess serum N-terminal proBNP (NT-proBNP) in systemic sclerosis patients and to establish whether it reflects the severity of RV overload.


Description:

Elevated serum brain natriuretic peptide (BNP) levels released from myocytes of ventricles upon stretch have been found in patients with isolated right ventricular (RV) pressure overload. However, limited data suggest that serum BNP may be elevated in patients with systemic sclerosis (SSc), especially with RV dysfunction. The aim of this study was to assess serum N-terminal proBNP (NT-proBNP) in SSc patients and to establish whether it reflects the severity of RV overload.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date April 2010
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Clinical diagnosis of systemic sclerosis

Exclusion Criteria:

- Cardiovascular disorders other than pulmonary hypertension

- Significant pulmonary function abnormalities

- Impaired renal function

Study Design

Observational Model: Defined Population, Primary Purpose: Screening, Time Perspective: Longitudinal


Locations

Country Name City State
Poland Michal Ciurzynski Warsaw Lindleya 4

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Warsaw

Country where clinical trial is conducted

Poland, 

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