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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02507843
Other study ID # 20150511
Secondary ID
Status Recruiting
Phase Phase 4
First received July 22, 2015
Last updated July 23, 2015
Start date January 2015
Est. completion date June 2017

Study information

Verified date July 2015
Source Shanghai Pulmonary Hospital, Shanghai, China
Contact JinFu Xu
Phone +86-13321922898
Email 13321922898@163.com
Is FDA regulated No
Health authority China: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

This study evaluates vitamin D as an adjunctive treatment in patients with non-Cystic Fibrosis bronchiectasis, which are combined with vitamin D deficiency. Half of participants will receive vitamin D supplementation, while the other half will receive placebo.


Description:

To define the therapeutic effect of Vitamin D in the treatment of non-Cystic Fibrosis bronchiectasis by means of a prospective randomized placebo-controlled double blind study with a follow-up of at least one year. To explore whether correction of Vitamin D deficiency by the oral supplementation of Vitamin D triggers the vitamin D receptors-mediated cathelicidin pathway and increases local or systemic concentrations of the natural antimicrobial polypeptide cathelicidin with enhanced eradication of bacteria.


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date June 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Diagnosis of non-Cystic fibrosis bronchiectasis by High Resolution CT

- Age 18 years or older

- Vitamin D deficiency [25(OH)D<20 ng/mL]

- Informed consent

Exclusion Criteria:

- Current active allergic bronchopulmonary or tuberculosis

- Diagnosis of any of the following: sarcoidosis, hyperparathyroidism, nephrolithiasis, pulmonary silicosis, Human Immunodeficiency Virus infection, liver failure, renal failure or malignancy

- Taking benzothiadiazine derivative, cardiac glycoside, carbamazepine, phenobarbital, phenytoin or primidone

- Taking dietary supplement or topical preparation containing vitamin D up to 2 months before first dose

- Treatment with any investigational medical product or device up to 4 months before first dose

- Breastfeeding, pregnant or planning a pregnancy

- Baseline corrected serum calcium > 2.65 mmol/L

- Baseline serum creatinine > 125 micromol/L

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Cholecalciferol
Oral Cholecalciferol(100000 IU) will be administered in Vitamin D group monthly for 6 months.
Placebo
Placebo will be administered in placebo group monthly for 6 months.

Locations

Country Name City State
China Shanghai Pulmonary Hospital , Tongji University Shanghai Shanghai

Sponsors (1)

Lead Sponsor Collaborator
Shanghai Pulmonary Hospital, Shanghai, China

Country where clinical trial is conducted

China, 

References & Publications (3)

Bartley J, Garrett J, Grant CC, Camargo CA Jr. Could vitamin d have a potential anti-inflammatory and anti-infective role in bronchiectasis? Curr Infect Dis Rep. 2013 Apr;15(2):148-57. doi: 10.1007/s11908-013-0321-9. — View Citation

Chalmers JD, McHugh BJ, Docherty C, Govan JR, Hill AT. Vitamin-D deficiency is associated with chronic bacterial colonisation and disease severity in bronchiectasis. Thorax. 2013 Jan;68(1):39-47. doi: 10.1136/thoraxjnl-2012-202125. Epub 2012 Oct 16. — View Citation

Martínez-García MÁ, de Gracia J, Vendrell Relat M, Girón RM, Máiz Carro L, de la Rosa Carrillo D, Olveira C. Multidimensional approach to non-cystic fibrosis bronchiectasis: the FACED score. Eur Respir J. 2014 May;43(5):1357-67. doi: 10.1183/09031936.0002 — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Time to first acute exacerbation one year No
Secondary total number of exacerbations per group one year No
Secondary percentage of patients with one or more exacerbations per year one year No
Secondary severity of diseases FACED(FEV1% predicted, age, chronic colonization by Pseudomonas aeruginosa, radiological extent of the disease, and dyspnea) score one year No
Secondary using of antibiotics types of antibiotics used during exacerbations one year No
Secondary quality of life the Quality of Life-Bronchiectasis (QOL-B) questionnaire one year No
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