Sickle Cell Anemia Clinical Trial
Verified date | July 2009 |
Source | The Baruch Padeh Medical Center, Poriya |
Contact | n/a |
Is FDA regulated | No |
Health authority | Israel: Ministry of Health |
Study type | Interventional |
The investigators would like to study the endothelial function in sickle cell patients without pulmonary hypertension in an in vivo method during a steady state condition before and after sildenafil treatment for 1 month, and to study the effects of this nitric oxide donor by measuring the Flow Mediated Dilatation, by measuring endothelial progenitor stem cells colonies, and by measuring the effect of therapy on markers of inflammation (cell adhesion molecules and cytokines).
Status | Withdrawn |
Enrollment | 15 |
Est. completion date | February 2010 |
Est. primary completion date | September 2009 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years to 60 Years |
Eligibility |
Inclusion Criteria: - patients with sickle cell anemia Exclusion Criteria: - patients with sickle cell anemia during acute crisis |
Allocation: Randomized, Endpoint Classification: Bio-availability Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Caregiver, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Israel | Baruch Padeh Poria Medical Center | Tiberias | Lower Galilee |
Lead Sponsor | Collaborator |
---|---|
The Baruch Padeh Medical Center, Poriya |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | endothelial function before and after viagra treatment to patients with sickle cell anemia without pulmonary hypertension | January 2009 till January 2011 | No |
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