Vitamin D as Treatment for Chronic Obstructive Pulmonary Disease (COPD)
Primary Purpose
Chronic Obstructive Pulmonary Disease
Status
Completed
Phase
Phase 4
Locations
Belgium
Study Type
Interventional
Intervention
D-cure
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring COPD
Eligibility Criteria
Inclusion Criteria:
- Primary diagnosis of COPD exacerbation
- Smoking history of at least ten pack years
- GOLD stage II, III and IV as assessed by a post-bronchodilator spirometry
- Informed consent
Exclusion Criteria:
- Tiffeneau index >70% or FEV1 >80%
- Hypercalcemia
- Sarcoidosis
- Newly discovered symptomatic osteoporosis (proven by DEXA and RX )
- Active cancer
Sites / Locations
- Katholieke Universiteit Leuven
- University hospital Leuven
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
1
2
Arm Description
Vitamin D (D-cure) will be administered by monthly oral intake. During a prospective follow-up period of one year, the patients will get the normal care with some additional tests for the study.
Placebo will be administered by monthly oral intake. During a prospective follow-up period of one year, the patients will get the normal care with some additional tests for the study.
Outcomes
Primary Outcome Measures
median time to next exacerbation.
Secondary Outcome Measures
Total number of exacerbations per group, number of exacerbations per patient per year, percentage of patients with one or more exacerbations per year, days of antibiotics and oral steroids, quality of life, FEV1, muscle force and survival.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00666367
Brief Title
Vitamin D as Treatment for Chronic Obstructive Pulmonary Disease (COPD)
Official Title
High Dosis of Vitamin D as Treatment for COPD.
Study Type
Interventional
2. Study Status
Record Verification Date
October 2009
Overall Recruitment Status
Completed
Study Start Date
January 2008 (undefined)
Primary Completion Date
June 2010 (Actual)
Study Completion Date
August 2010 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
KU Leuven
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This project aims to explore the relationship between Vitamin D deficiency and COPD progression via a prospective randomized placebo-controlled study. For this purpose, study was powered to 120 patients hospitalized with an exacerbation of COPD randomly assigned to a monthly oral dose of Vitamin D versus placebo. Taking into account dropouts, 182 patients are randomized during the course of the study
Detailed Description
Principal objective: To define the therapeutic effect of Vitamin D in the chronic maintenance treatment of COPD by means of a prospective randomized placebo-controlled double blind study of 182 patients with a follow-up of at least one year. Primary endpoint is the median time to next exacerbation. Secondary endpoints are total number of exacerbations per group, number of exacerbations per patient per year, percentage of patients with one or more exacerbations per year, days of antibiotics and oral steroids, quality of life, FEV1, muscle force and survival.
Other objectives: First, to investigate the role of local and systemic levels of 25-OHD and 1,25-(OH)2D on the intensity and prevalence of bacterial colonisation, inflammatory markers, proteases and markers of oxidative stress in induced sputa and exhaled air. Second, to explore whether correction of Vitamin D deficiency by the oral supplementation of Vitamin D triggers the VDR-mediated cathelicidin pathway and increases local or systemic concentrations of the natural antimicrobial polypeptide cathelicidin with enhanced eradication of bacteria.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
COPD
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
182 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Active Comparator
Arm Description
Vitamin D (D-cure) will be administered by monthly oral intake. During a prospective follow-up period of one year, the patients will get the normal care with some additional tests for the study.
Arm Title
2
Arm Type
Placebo Comparator
Arm Description
Placebo will be administered by monthly oral intake. During a prospective follow-up period of one year, the patients will get the normal care with some additional tests for the study.
Intervention Type
Drug
Intervention Name(s)
D-cure
Other Intervention Name(s)
license number: D-cure: 465S37F11
Intervention Description
4 ml of D-cure (SMB oral intake) in syringe Exacta-Med Oral Dispenser.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Product number: Arachidis oleum raffinatum: *FA072892*
Intervention Description
4 ml of Arachidis oleum raffinatum Ph. Eur. in syringe Med Oral Dispenser.
Primary Outcome Measure Information:
Title
median time to next exacerbation.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Total number of exacerbations per group, number of exacerbations per patient per year, percentage of patients with one or more exacerbations per year, days of antibiotics and oral steroids, quality of life, FEV1, muscle force and survival.
Time Frame
1 year
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Primary diagnosis of COPD exacerbation
Smoking history of at least ten pack years
GOLD stage II, III and IV as assessed by a post-bronchodilator spirometry
Informed consent
Exclusion Criteria:
Tiffeneau index >70% or FEV1 >80%
Hypercalcemia
Sarcoidosis
Newly discovered symptomatic osteoporosis (proven by DEXA and RX )
Active cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wim Janssens, Prof.
Organizational Affiliation
KU Leuven
Official's Role
Principal Investigator
Facility Information:
Facility Name
Katholieke Universiteit Leuven
City
Leuven
State/Province
Flanders
ZIP/Postal Code
3000
Country
Belgium
Facility Name
University hospital Leuven
City
Leuven
State/Province
Flanders
ZIP/Postal Code
3000
Country
Belgium
12. IPD Sharing Statement
Citations:
PubMed Identifier
35236342
Citation
Serre J, Tanjeko AT, Mathyssen C, Heigl T, Sacreas A, Cook DP, Verbeken E, Maes K, Verhaegen J, Pilette C, Vanoirbeek J, Gysemans C, Mathieu C, Vanaudenaerde B, Janssens W, Gayan-Ramirez G. Effects of repeated infections with non-typeable Haemophilus influenzae on lung in vitamin D deficient and smoking mice. Respir Res. 2022 Mar 2;23(1):40. doi: 10.1186/s12931-022-01962-6.
Results Reference
derived
PubMed Identifier
22250141
Citation
Lehouck A, Mathieu C, Carremans C, Baeke F, Verhaegen J, Van Eldere J, Decallonne B, Bouillon R, Decramer M, Janssens W. High doses of vitamin D to reduce exacerbations in chronic obstructive pulmonary disease: a randomized trial. Ann Intern Med. 2012 Jan 17;156(2):105-14. doi: 10.7326/0003-4819-156-2-201201170-00004.
Results Reference
derived
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Vitamin D as Treatment for Chronic Obstructive Pulmonary Disease (COPD)
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