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The effect of vitamin D deficiency treatment on chronic obstructive pulmonary diseasepatients

Not Applicable
Conditions
Chronic Obstructive Pulmonary Disease.
Other chronic obstructive pulmonary disease
Registration Number
IRCT2013072114085N2
Lead Sponsor
Vice chancellor of research ,Guilan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
50
Inclusion Criteria

The inclusion of study criteria are as following : the proof of COPD diagnosis according to clinical conditions and its approval with spirometry based on GOLD ; low serum levels of 25-hydroxyvitamin D (10-30) as insufficiency. The study exclusion criteria : hypercalcemia ; ca more than10.3 ; sarcoidosis (according to diagnosis and clinical examination of pulmonary subspecialty ; cancer (asking the patient) ; osteoprosis that has recently been diagnosed (asking the patient) ; long term use of azithromycin (asking the patient) ; serum 25-hydroxy vitamin D levels less than 10 as deficiency ; thyroid and parathyroid diseases.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The rate of change in COPD stage according to GOLD stages. Timepoint: The time of study inclusion and one month later and 6 months later. Method of measurement: Spirometry.;Evaluation of quality of life of patients. Timepoint: The time of study inclusion and one month later and 6 months later. Method of measurement: CAT Questionnair.;Serum levels of 25-hydroxyvitamin D. Timepoint: The time of study inclusion and one month later and 6 months later. Method of measurement: Measurement of serum levels of 25-hydroxyvitamin D.
Secondary Outcome Measures
NameTimeMethod
Mortality. Timepoint: During study. Method of measurement: Recording in patients’ information forms.;The duration of taking Systemic steroids and antibiotics. Timepoint: During the study. Method of measurement: Recording in patients’ information forms.;Number of exacerbations. Timepoint: duringt study. Method of measurement: recording in patients’ information forms.;The median time of the occurrence of the first exacerbation during the study. Timepoint: during study. Method of measurement: recording in patients’ information forms.
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