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Vitamin D for Enhancing the Immune System in Cystic Fibrosis (DISC Study) (DISC)

Primary Purpose

Cystic Fibrosis, Respiratory Tract Infections

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Cholecalciferol
Sponsored by
Emory University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cystic Fibrosis focused on measuring vitamin D, cholecalciferol, cystic fibrosis, respiratory tract infection, immunity, intervention studies, inflammation, dietary supplements, alpha-Defensins, Cytokines, mortality, biological markers, Biomedical Research

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult and adolescent CF patients
  • age >16 years
  • admitted to the inpatient hospital setting for a pulmonary exacerbation of cystic fibrosis
  • enrolled within 72 hours of admission
  • able to tolerate oral medications
  • expected to survive hospitalization

Exclusion Criteria:

  • Inability to obtain or declined informed consent from the subject and/or legally authorized representative
  • History of serum 25(OH)D >55 ng/mL in the past 12 months
  • History of serum 25(OH)D <10 ng/mL in the past 12 months
  • Current intake of more than 2,000 IU of vitamin D
  • intake of 2,000 IU of vitamin D or its equivalent weekly dose (14,000 IU) for more than 1 week at any time within the past 60 days or intake of greater than vitamin D 10,000 IU once at anytime in the past 60 days
  • Pregnancy or plans to become pregnant during the course of the study (12 months)
  • History of disorders associated with hypercalcemia including parathyroid disease
  • Current hypercalcemia (albumin-corrected serum calcium >10.8 mg/dL or ionized calcium >5.2 mg/dL)
  • History of nephrolithiasis
  • Chronic kidney disease worse than stage III (<60 ml/min)
  • Oral or intravenous glucocorticoid use currently or in the past month
  • History of lung transplantation or awaiting lung transplant
  • patient in hospice care
  • FEV1% predicted <20%
  • Current significant hepatic dysfunction total bilirubin > 2.5 mg/dL with direct bilirubin > 1.0 mg/dL
  • Current use of cytotoxic or immunosuppressive drugs
  • History of AIDS
  • History of illicit drug abuse (defined as history of enrollment into a drug rehabilitation program or hospital visits due to drug use within the past 3 years or any use of the following drugs in the past 6 months (cocaine, opiates, amphetamines, marijuana) or any positive toxicology screen for (cocaine, opiates, amphetamines, marijuana)
  • Previous enrollment in the study
  • Current enrollment in another intervention trial
  • Too ill to participate in study based on investigator's or study team's opinion

Sites / Locations

  • University of Alabama at Birmingham
  • Emory Hospital
  • University of Iowa
  • University of Cincinnati
  • Case Western Reserve University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Cholecalciferol (Vitamin D3)

Placebo

Arm Description

Patients will be given 250,000 IU cholecalciferol in one bolus oral dose while they are in the hospital. Three months after the initial bolus dose, patients will take 50,000 IU oral cholecalciferol every other week for 9 months.

Patients will be given placebo pills in one bolus oral dose while they are in the hospital. Three months after the initial bolus dose, patients will take a placebo pill every other week for 9 months.

Outcomes

Primary Outcome Measures

Study enrollment to next pulmonary exacerbation requiring any antibiotics, hospitalization or death.

Secondary Outcome Measures

inflammation
We will examine whether the high-dose vitamin D treatment regimen decreases the pro-inflammatory cytokines, IL-6, IL-8, and TNF- α.
mortality as a separate outcome
re-hospitalization as a separate outcome
anti-microbial proteins
We will examine whether the high-dose vitamin D treatment regimen increases cathelicidin and hBD-2 mRNA expression in both peripheral blood mononuclear cells (PBMCs) and induced sputum (by quantitative PCR).
Lung function
We will examine whether high dose vitamin D improves serial lung function, as measured by FEV1
Antibiotic use
Rates of pulmonary exacerbation requiring antibiotics due to presumed infection after 12 month
glucose metabolism
Rates of new onset diabetes and mean glucose values in each group

Full Information

First Posted
August 29, 2011
Last Updated
July 11, 2017
Sponsor
Emory University
Collaborators
Cystic Fibrosis Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT01426256
Brief Title
Vitamin D for Enhancing the Immune System in Cystic Fibrosis (DISC Study)
Acronym
DISC
Official Title
Vitamin D for Enhancing the Immune System in Cystic Fibrosis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
October 2011 (undefined)
Primary Completion Date
April 2017 (Actual)
Study Completion Date
July 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University
Collaborators
Cystic Fibrosis Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is determine if high-dose vitamin D supplementation improves clinical outcomes related to lung function and immunity in patients with Cystic Fibrosis who are admitted to the hospital with an acute lung infection.
Detailed Description
Patients with Cystic Fibrosis (CF) have a shorter life span than the general population due to complications with lung infections, which eventually progress to lung failure. New research has suggested that high levels of vitamin D may be protective against lung infections and may promote the action of anti-bacterial proteins needed to ward off infections. Research has also suggested that high vitamin D levels are linked to lower mortality rates; however these hypotheses have not been adequately studied in patients with CF. An investigation of the effects of vitamin D supplementation is of particular interest in this population because patients with CF generally have high rates of vitamin D deficiency. The investigators have preliminary data from a previous study suggesting that vitamin D supplementation in patients with CF lowers markers of inflammation, promotes anti-bacterial proteins, and reduces mortality. In this proposed multi-center study the investigators will examine the effects of a high dose vitamin D supplementation on patients with CF who are admitted to the hospital for lung infection. The investigators will use a randomized, placebo-controlled trial design to determine if mortality and infection rates over 1 year are reduced in patients who receive the high-dose vitamin D supplementation compared to those who receive placebo. The investigators will also determine if vitamin D affects markers of inflammation and anti-bacterial proteins, as well as CF-related clinical outcomes, such as lung function. The investigators plan to recruit 280 adults and adolescents with CF (ages > 16yrs), with approximately 150 subjects recruited at Emory (Emory University Hospital and Children's Healthcare of Atlanta). Participants will initially be seen by the study researchers during the first week of in-patient hospitalization, and they will be followed over the course of one year during their regularly-scheduled out-patient CF clinic visits. The treatment group will receive an initial oral bolus dose of 250,000 IU vitamin D, and at 3 months follow-up they will receive 50,000 IU vitamin D every other week. Current CF Guidelines for vitamin D supplementation recommend a daily intake of 800 IU of vitamin D per day, therefore in addition to the vitamin D or placebo they receive at the beginning of the study and at 3 months, all participants will receive 800 IU of vitamin D daily. If our hypotheses are correct, this study has potential for reducing infection and promoting survival in patients with CF using vitamin D, a relatively inexpensive supplement.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cystic Fibrosis, Respiratory Tract Infections
Keywords
vitamin D, cholecalciferol, cystic fibrosis, respiratory tract infection, immunity, intervention studies, inflammation, dietary supplements, alpha-Defensins, Cytokines, mortality, biological markers, Biomedical Research

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
91 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Cholecalciferol (Vitamin D3)
Arm Type
Experimental
Arm Description
Patients will be given 250,000 IU cholecalciferol in one bolus oral dose while they are in the hospital. Three months after the initial bolus dose, patients will take 50,000 IU oral cholecalciferol every other week for 9 months.
Arm Title
Placebo
Arm Type
No Intervention
Arm Description
Patients will be given placebo pills in one bolus oral dose while they are in the hospital. Three months after the initial bolus dose, patients will take a placebo pill every other week for 9 months.
Intervention Type
Dietary Supplement
Intervention Name(s)
Cholecalciferol
Other Intervention Name(s)
Vitamin D
Intervention Description
Bolus dose of 250,000 IU during hospitalization + maintenance dose of 50,000 IU vitamin D every other week to be initiated 3 months after bolus dose
Primary Outcome Measure Information:
Title
Study enrollment to next pulmonary exacerbation requiring any antibiotics, hospitalization or death.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
inflammation
Description
We will examine whether the high-dose vitamin D treatment regimen decreases the pro-inflammatory cytokines, IL-6, IL-8, and TNF- α.
Time Frame
12 months
Title
mortality as a separate outcome
Time Frame
12 months
Title
re-hospitalization as a separate outcome
Time Frame
12 months
Title
anti-microbial proteins
Description
We will examine whether the high-dose vitamin D treatment regimen increases cathelicidin and hBD-2 mRNA expression in both peripheral blood mononuclear cells (PBMCs) and induced sputum (by quantitative PCR).
Time Frame
12 months
Title
Lung function
Description
We will examine whether high dose vitamin D improves serial lung function, as measured by FEV1
Time Frame
12 months
Title
Antibiotic use
Description
Rates of pulmonary exacerbation requiring antibiotics due to presumed infection after 12 month
Time Frame
12 months
Title
glucose metabolism
Description
Rates of new onset diabetes and mean glucose values in each group
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
16 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult and adolescent CF patients age >16 years admitted to the inpatient hospital setting for a pulmonary exacerbation of cystic fibrosis enrolled within 72 hours of admission able to tolerate oral medications expected to survive hospitalization Exclusion Criteria: Inability to obtain or declined informed consent from the subject and/or legally authorized representative History of serum 25(OH)D >55 ng/mL in the past 12 months History of serum 25(OH)D <10 ng/mL in the past 12 months Current intake of more than 2,000 IU of vitamin D intake of 2,000 IU of vitamin D or its equivalent weekly dose (14,000 IU) for more than 1 week at any time within the past 60 days or intake of greater than vitamin D 10,000 IU once at anytime in the past 60 days Pregnancy or plans to become pregnant during the course of the study (12 months) History of disorders associated with hypercalcemia including parathyroid disease Current hypercalcemia (albumin-corrected serum calcium >10.8 mg/dL or ionized calcium >5.2 mg/dL) History of nephrolithiasis Chronic kidney disease worse than stage III (<60 ml/min) Oral or intravenous glucocorticoid use currently or in the past month History of lung transplantation or awaiting lung transplant patient in hospice care FEV1% predicted <20% Current significant hepatic dysfunction total bilirubin > 2.5 mg/dL with direct bilirubin > 1.0 mg/dL Current use of cytotoxic or immunosuppressive drugs History of AIDS History of illicit drug abuse (defined as history of enrollment into a drug rehabilitation program or hospital visits due to drug use within the past 3 years or any use of the following drugs in the past 6 months (cocaine, opiates, amphetamines, marijuana) or any positive toxicology screen for (cocaine, opiates, amphetamines, marijuana) Previous enrollment in the study Current enrollment in another intervention trial Too ill to participate in study based on investigator's or study team's opinion
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vin Tangpricha, MD, PhD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Emory Hospital
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Facility Name
University of Iowa
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States
Facility Name
University of Cincinnati
City
Cincinnati
State/Province
Ohio
ZIP/Postal Code
45267
Country
United States
Facility Name
Case Western Reserve University
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18284636
Citation
Wolfenden LL, Judd SE, Shah R, Sanyal R, Ziegler TR, Tangpricha V. Vitamin D and bone health in adults with cystic fibrosis. Clin Endocrinol (Oxf). 2008 Sep;69(3):374-81. doi: 10.1111/j.1365-2265.2008.03216.x. Epub 2008 Feb 11.
Results Reference
background
PubMed Identifier
19336509
Citation
Khazai NB, Judd SE, Jeng L, Wolfenden LL, Stecenko A, Ziegler TR, Tangpricha V. Treatment and prevention of vitamin D insufficiency in cystic fibrosis patients: comparative efficacy of ergocalciferol, cholecalciferol, and UV light. J Clin Endocrinol Metab. 2009 Jun;94(6):2037-43. doi: 10.1210/jc.2008-2012. Epub 2009 Mar 31.
Results Reference
background
PubMed Identifier
19342361
Citation
Pepper KJ, Judd SE, Nanes MS, Tangpricha V. Evaluation of vitamin D repletion regimens to correct vitamin D status in adults. Endocr Pract. 2009 Mar;15(2):95-103. doi: 10.4158/EP.15.2.95.
Results Reference
background
PubMed Identifier
30793177
Citation
Tangpricha V, Lukemire J, Chen Y, Binongo JNG, Judd SE, Michalski ES, Lee MJ, Walker S, Ziegler TR, Tirouvanziam R, Zughaier SM, Chesdachai S, Hermes WA, Chmiel JF, Grossmann RE, Gaggar A, Joseph PM, Alvarez JA. Vitamin D for the Immune System in Cystic Fibrosis (DISC): a double-blind, multicenter, randomized, placebo-controlled clinical trial. Am J Clin Nutr. 2019 Mar 1;109(3):544-553. doi: 10.1093/ajcn/nqy291. Erratum In: Am J Clin Nutr. 2023 May;117(5):1048.
Results Reference
derived

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Vitamin D for Enhancing the Immune System in Cystic Fibrosis (DISC Study)

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