Status:
WITHDRAWN
Sildenafil Trial in Children and Young Adults With CF
Lead Sponsor:
Children's Hospital Medical Center, Cincinnati
Conditions:
Cystic Fibrosis With Mild to Moderate Lung Disease
CMRI of Lung Perfusion
Eligibility:
All Genders
8-21 years
Phase:
PHASE1
PHASE2
Brief Summary
Cystic Fibrosis (CF), the most common inherited disease in Caucasians, is characterized by chronic pulmonary inflammation and progressive loss of gas exchange units that eventually results in respirat...
Eligibility Criteria
Inclusion
- Inclusion Criteria
- Research subjects must meet the following inclusion criteria:
- Age 8 years to age 21 years
- Weight \> 20kg
- Diagnosis of cystic fibrosis confirmed by a prior sweat chloride evaluation of \> 60 mmol/liter or by two identified CFTR mutations on genetic analysis
- Able to perform acceptable and repeatable spirometry per American Thoracic Society/European Respiratory Society (ATS/ERS) joint consensus criteria.
- Have valid spirometry data for at least 3 years
- Must have mild to moderate lung disease (Mild lung disease will be defined as an FEV1%p of 80-99% predicted. Moderate lung disease will be defined as an FEV1%p of 60-79% predicted.)
- If under the age of 18, the subject must assent to participation in the study, and the subject's parent or guardian must be able to give written informed consent and comply with the requirements of the study protocol
- If 18 years of age or older, the subject must be able to give written parental permission and comply with the requirements of the study protocol
- For female subjects: negative serum pregnancy test and must be willing to use contraception during study participation
- Able to tolerate MRI without sedation
- Subjects who are on alternating monthly on/off cycles of inhaled antibiotics must be willing to be off of inhaled antibiotic therapy for one "on" cycle.
- Must be currently enrolled in CCHMC IRB#: 2008-0926
- Normal Vitamin K status (PT/IND, PIVKA, etc) at screening
- Exclusion Criteria
- Research subjects will be excluded from the study based on:
- History of CF-related liver disease with portal hypertension
- Currently smoking cigarettes or other tobacco products
- Use of daytime oxygen supplementation
- Previous organ transplantation
- Unstable or uncontrolled hypertension
- Ongoing use of oral corticosteroids
- For female subjects: pregnancy or lactation and unwillingness to use contraception during study participation
- Any hemodynamically significant congenital or acquired cardiac disease or significant cardiomyopathy, hematologic disease (i.e. hemoglobinopathies), or pulmonary disease associated with an increased risk of pulmonary perfusion defects or pulmonary hypertension other than as an outcome of CF
- History of renal and/or hepatic insufficiency, defined as cystatin-C level that exceeds normal range and a previous diagnosis of liver cirrhosis.
- History of uncontrolled asthma defined as oral steroid dependent
- History of hypersensitivity to gadolinium (Magnevist)
- Contraindications specific to MRI including a history of claustrophobia, cardiac pacemaker, or other non-MRI compatible surgical implants (This includes neuro-stimulators containing electrical circuitry, or which generate electrical signals and/or have moving metal parts, and metal orthopedic pins or plates. The research coordinator and/or the MRI technologist will screen all subjects using the standard checklist of medical history and safety questions used by the Radiology Department in routine clinical scans.)
- Daily use of montelukast and ibuprofen
- Use of nitrate medicines or other drugs known to have unsafe interactions with Sildenafil
- Known allergy to Sildenafil
- Inability to comply with study procedures
- History of the following:
- Tinnitus or hearing impairment
- CF exacerbation within the preceding two months
- Ulcer, severe gastritis, or prior GI bleed
- Recurrent epistaxis
- Diabetes or abnormal OGTT (risk of retinal hemorrhage with sildenafil is highest in diabetics)
- Laboratory Exclusion Criteria for research subjects (based on history or blood work before first MRI):
- Positive sputum, epiglottic, or bronchoalveolar lavage culture for Mycobacterium abscessus during the 2 years prior to enrollment
- A positive serum pregnancy test
- Serum creatinine \> two times the upper limit of normal for age
- A serum Cystatin C \< 60 ml/min/1.73m2
- Vitamin K outside of normal range
Exclusion
Key Trial Info
Start Date :
August 1 2012
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
December 1 2012
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT01194232
Start Date
August 1 2012
End Date
December 1 2012
Last Update
December 11 2012
Active Locations (0)
Enter a location and click search to find clinical trials sorted by distance.
No Results Found
We couldn’t find results for the location/zipcode entered or within the selected range. Please check your input or adjust your search.