Cystic Fibrosis Clinical Trial
Official title:
Open-label Vitamin D Trial for Patients With Cystic Fibrosis and Allergic Bronchopulmonary Aspergillosis
Verified date | March 2018 |
Source | University of Pittsburgh |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to see if giving people with CF and ABPA enough vitamin D to make their blood levels of the vitamin higher, will reduce the allergic response in their body and make the symptoms caused by ABPA better.
Status | Completed |
Enrollment | 7 |
Est. completion date | September 2013 |
Est. primary completion date | September 2013 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 12 Years and older |
Eligibility |
Inclusion Criteria: 1. Male or female = 12 years of age at enrollment 2. Confirmed diagnosis of CF based on the following criteria: 1. One or more clinical features consistent with the CF phenotype AND (b or c) 2. Positive sweat chloride > 60 mEq/liter (by pilocarpine iontophoresis) 3. two identifiable mutations consistent with CF 3. Written informed consent (and assent when applicable) obtained from subject or subject's legal representative and ability for subject to comply with the requirements of the study. 4. Clinically stable at enrollment as assessed by the site investigator 5. Past or present respiratory culture positive for Aspergillus fumigatus 6. IgE = 250 and/or presence of class II or higher aspergillus specific IgE on enrollment 7. Ability to comply with medication use, study visits and study procedures as judged by the site investigator - Exclusion Criteria: - 1. Systemic corticosteroids (1 mg/kg if < 20 kg or > 20 mg of prednisone per day),. 2. Investigational drug use within 30 days of screening 3. Laboratory abnormalities at screening a. Serum Calcium > 11 mg/dl b. 25(OH) D > 50 ng/ml at screening. c. Creatinine = 1.5, or estimated GFR <60 by Cockcroft-Gault or MDRD equation. d. LFT= 3xULN 4. History of transplantation or currently on lung transplant list 5. Positive serum pregnancy test at screening (to be performed on all post-menarche females) 6. Pregnant, breastfeeding, or if post-menarche female, unwilling to practice birth control during participation in the study 7. Presence of a condition or abnormality that in the opinion of the site investigator would compromise the safety of the subject or the quality of the data 8. Diagnosis of HIV and a CD4+ T cell count below 500 cells/ml or active hepatitis B or C infection. 9. Undergoing therapy for non-tuberculous mycobacterial infection |
Country | Name | City | State |
---|---|---|---|
United States | Children's Hospital of Pittsburgh of UPMC | Pittsburgh | Pennsylvania |
United States | Comprehensive Lung Center - Falk Clinic | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pittsburgh | National Heart, Lung, and Blood Institute (NHLBI) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of Participants With Aspergillus Induced IL-13 Responses in CD4+ T-cells | To test the hypothesis that supplementation with Vitamin D in CF patients with ABPA will reduce Aspergillus induced IL-13 responses in peripheral CD4+ T-cells. Response confirmed for each individual patient and recorded as number of participants with response. | 6 months | |
Secondary | Change in Patient Total IgE Levels | To test the hypothesis that supplementation with Vitamin D in CF patients with ABPA will reduce total IgE levels by the end of the 24-week period | 6 months | |
Secondary | Change in Patient Aspergillus Specific IgE Levels | To test the hypothesis that supplementation with Vitamin D in CF patients with ABPA will reduce aspergillus specific IgE levels by the end of the 24-week period | 6 months |
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