Non-Invasive Diagnostic and Functional Evaluation of Cardiac Involvement in Patients With Systemic Sclerosis
The recruitment status of this study is unknown because the information has not been verified recently.
Verified March 2006 by Medical University of Warsaw.
Recruitment status was Recruiting
Recruitment status was Recruiting
Sponsor:
Medical University of Warsaw
Information provided by:
Medical University of Warsaw
ClinicalTrials.gov Identifier:
NCT00453752
First received: March 28, 2007
Last updated: NA
Last verified: March 2006
History: No changes posted
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Purpose
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.
| Condition |
|---|
|
Systemic Sclerosis |
| Study Type: | Observational |
| Study Design: | Observational Model: Defined Population Primary Purpose: Screening Time Perspective: Longitudinal Time Perspective: Prospective |
Resource links provided by NLM:
Further study details as provided by Medical University of Warsaw:
| Estimated Enrollment: | 100 |
| Study Start Date: | April 2006 |
| Estimated Study Completion Date: | April 2010 |
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.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Clinical diagnosis of systemic sclerosis
Exclusion Criteria:
- Cardiovascular disorders other than pulmonary hypertension
- Significant pulmonary function abnormalities
- Impaired renal function
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00453752
Contacts
| Contact: Ciurzyński Michał, M.D, Ph.D | +48 22 502 11 44 | mciurzyn@amwaw.edu.pl |
| Contact: Piotr Pruszczyk, M.D, Ph.D. | +48 22 501 11 44 | ppruszczyk@amwaw.edu.pl |
Locations
| Poland | |
| Michał Ciurzyński | Recruiting |
| Warsaw, Lindleya 4, Poland, 02-005 | |
| Contact: Michał Ciurzyński, M.D, Ph.D +48 22 502 11 44 mciurzyn@amwaw.edu.pl | |
Sponsors and Collaborators
Medical University of Warsaw
Investigators
| Principal Investigator: | Michał Ciurzyński, M.D., Ph.D | Medical University of Warsaw |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00453752 History of Changes |
| Other Study ID Numbers: | KB/66/2006 |
| Study First Received: | March 28, 2007 |
| Last Updated: | March 28, 2007 |
| Health Authority: | Poland: Ministry of Health |
Keywords provided by Medical University of Warsaw:
|
systemic sclerosis pulmonary hypertension echocardiography N-Terminal proBNP |
Additional relevant MeSH terms:
|
Scleroderma, Systemic Scleroderma, Diffuse Sclerosis |
Connective Tissue Diseases Skin Diseases Pathologic Processes |
ClinicalTrials.gov processed this record on May 23, 2013