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24 studies found for:    Cystic Fibrosis | Open Studies | NIH, U.S. Fed
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Rank Status Study
1 Recruiting Studying Patients With Cystic Fibrosis and Other Pulmonary and Pancreatic Disorders
Condition: Cystic Fibrosis
Intervention:
2 Recruiting Blood Flow and Vascular Function in Cystic Fibrosis
Condition: Cystic Fibrosis
Interventions: Drug: Acute (1 hour) Sildenafil;   Drug: Sub-Chronic (4 weeks) Sildenafil;   Drug: Placebo
3 Recruiting Mapping Chemical and Microbiological Heterogeneity Throughout Explanted Cystic Fibrosis Lung Specimens
Condition: Cystic Fibrosis
Intervention:
4 Not yet recruiting MRI to Characterize and Predict CF Liver Disease in PUSH Cohort
Conditions: Cystic Fibrosis Liver Disease;   Pancreatic Insufficiency
Intervention: Procedure: MRI
5 Recruiting Comparing Chest Images From MRI to CT in Patients With Cystic Fibrosis (CF)
Condition: Cystic Fibrosis
Intervention:
6 Recruiting BioEnergetics and Metabolomics in Cystic Fibrosis
Condition: Cystic Fibrosis
Intervention:
7 Recruiting OPTIMIZing Treatment for Early Pseudomonas Aeruginosa Infection in Cystic Fibrosis
Condition: Cystic Fibrosis
Interventions: Drug: azithromycin;   Drug: placebo;   Drug: Tobramycin solution for inhalation
8 Recruiting The Role of Bacteria and Genetic Variations in Cystic Fibrosis
Condition: Lung Diseases
Intervention:
9 Recruiting Using MRI to Observe Lung Changes in Infants With CF Compared to Infants Without CF
Condition: Cystic Fibrosis
Intervention:
10 Not yet recruiting Multilevel Models of Therapeutic Response in the Lungs
Condition: Cystic Fibrosis
Interventions: Drug: Hypertonic Saline;   Drug: Isotonic Saline;   Drug: Indium-DTPA;   Drug: Technetium Sulfur Colloid
11 Recruiting Monitoring Response to Orkambi in Cystic Fibrosis Lung Disease by Inhaled Xenon MRI
Condition: Cystic Fibrosis
Intervention: Drug: Hyperpolarized Xenon
12 Recruiting UAB HRFD Core Center: Core A: The Hepato/Renal Fibrocystic Diseases Translational Resource
Conditions: Hepato/Renal Fibrocystic Disease;   Autosomal Recessive Polycystic Kidney Disease;   Joubert Syndrome;   Bardet Biedl Syndrome;   Meckel-Gruber Syndrome;   Congenital Hepatic Fibrosis;   Caroli Syndrome;   Oro-Facial-Digital Syndrome Type I;   Nephronophthisis;   Glomerulocystic Kidney Disease
Intervention:
13 Recruiting Role of Toxins in Lung Infections Caused by Pseudomonas Aeruginosa
Conditions: Pseudomonas Infection;   Cystic Fibrosis
Intervention:
14 Recruiting Natural History of Bronchiectasis
Conditions: Bronchiectasis;   Cystic Fibrosis;   Autoimmune Disease;   Common Variable Immunodeficiency
Intervention:
15 Recruiting Muscle Accrual and Function in Cystic Fibrosis-Impact of Glucose Intolerance
Condition: Cystic Fibrosis
Intervention:
16 Recruiting Biomarkers of Injury and Destruction in the Cystic Fibrosis Lung
Condition: Cystic Fibrosis
Intervention:
17 Recruiting Study of Mycobacterial Infections
Conditions: Atypical Mycobacterium Infections;   Cystic Fibrosis;   Job's Syndrome
Intervention:
18 Recruiting Testing the Effect of Adding Chronic Oral Azithromycin to Inhaled Tobramycin in People With CF
Condition: Cystic Fibrosis
Interventions: Drug: azithromycin;   Drug: placebo (for azithromycin);   Drug: inhaled tobramycin
19 Recruiting Genetic Modifiers of Cystic Fibrosis Related Diabetes
Condition: Cystic Fibrosis Related Diabetes
Intervention:
20 Recruiting Role of Genetic Factors in the Development of Lung Disease
Conditions: Cystic Fibrosis;   Sarcoidosis;   Tuberous Sclerosis;   Asthma
Intervention:

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Study has passed its completion date and status has not been verified in more than two years.