Status:
COMPLETED
Sildenafil to Improve Exercise Capacity in People With Thalassemia and Pulmonary Hypertension
Lead Sponsor:
Carelon Research
Collaborating Sponsors:
National Heart, Lung, and Blood Institute (NHLBI)
Conditions:
Thalassemia
Hypertension, Pulmonary
Eligibility:
All Genders
7+ years
Phase:
PHASE2
PHASE3
Brief Summary
Thalassemia is an inherited blood disorder that can result in mild to severe anemia. Many people with thalassemia also have pulmonary hypertension, which is high blood pressure in the arteries in the ...
Detailed Description
Thalassemia is an inherited blood disorder in which the body makes an abnormal form of hemoglobin-the protein in red blood cells that carries oxygen. A potential complication of thalassemia is pulmona...
Eligibility Criteria
Inclusion
- Inclusion Criteria for All Participants:
- Alpha, beta, or E-beta thalassemia confirmed by hemoglobin (Hb)-electrophoresis or molecular diagnosis
- Inclusion Criteria for Participants with Pulmonary Hypertension:
- Pulmonary hypertension, defined as a tricuspid regurgitant jet (TRjet) velocity by Doppler echocardiography greater than 2.5 m/s
- Inclusion Criteria for Participants without Pulmonary Hypertension:
- Lack of pulmonary hypertension, defined as TRjet velocity by Doppler echocardiography less than 2.5 m/s
- Exclusion Criteria:
- Pregnant or breastfeeding
- Hypersensitivity to arginine or sildenafil, based on prior use
- Any of the following medical conditions:
- Severe kidney insufficiency, defined as use of hemodialysis or serum creatinine at levels greater than 2.5 mg/dL at the time of screening
- Cardiac disease with adjustment of cardiac medications in the 60 days before study entry
- Symptomatic coronary artery disease, as indicated by a history of chest pain, angina, claudication, or surgery to treat coronary artery disease in the 1 year before study entry
- Stroke, defined as a new focal neurological deficit lasting more than 24 hours in the 45 days before study entry
- New diagnosis of pulmonary embolism by ventilation-perfusion scan, angiography, or any other technique in the 90 days before study entry
- History of retinal detachment or retinal hemorrhage in the 180 days before study entry
- Use of nitrate-based vasodilators, prostacyclin (inhaled, subcutaneous, or intravenous), endothelin antagonists, or any other medication for pulmonary hypertension
- Acute asthma exacerbation requiring use of prednisone in the 60 days before study entry
- Initiation or dosage increase of calcium channel blockers in the 30 days before study entry
- Initiation of any other cardiac or pulmonary medication in the 90 days before study entry
- Presence of any other condition, which in the opinion of the investigator, would make the person unsuitable for enrollment or could interfere with compliance in the study, including but not limited to alcohol or drug abuse
- No measurable TRjet on Doppler echocardiography (i.e., presence of pulmonary hypertension cannot be confirmed or ruled out)
Exclusion
Key Trial Info
Start Date :
March 1 2009
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
November 1 2010
Estimated Enrollment :
27 Patients enrolled
Trial Details
Trial ID
NCT00872170
Start Date
March 1 2009
End Date
November 1 2010
Last Update
February 21 2014
Active Locations (1)
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1
Children's Hospital and Research Institute Oakland
Oakland, California, United States, 94609