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Role of vitamin D in lung function parameters in children of bronchial asthma

Efficacy and Safety of Oral Vitamin D supplementation on pulmonary function parameters assessed by forced oscillation technique in children with bronchial asthma: A pilot, double blind, randomized trial ? - NA

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/02/062246
Enrollment
50
Registered
2024-02-05
Start date
Unknown
Completion date
Unknown
Last updated
2024-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: J452- Mild intermittent asthma

Interventions

Intervention1: Vitamin D: Oral Vitamin D 2000 IU per day for 3 months. Control Intervention1: Placebo of same form.: Placebo per oral daily for 3 months

Sponsors

All India Institute of Medical Sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Patients with bronchial asthma diagnosed based on GINA 2023 criteria or ERS/ATS criteria • Inclusion criteria A) Children with newly diagnosed Bronchial Asthma based on the following criteria. 1) Clinical feature suggestive of bronchial asthma as per GINA 2023 2) Clinical feature and or bronchodilator responsiveness based on FOT/Spirometry as per ERS/ATS criteria B) Children who have been treated for Bronchial Asthma previously will be eligible for inclusion if they are off maintenance therapy (i.e Inhaled Corticosteroids) since last 3 months. Stratification of study population: A) Newly diagnosed Vs Previously diagnosed

Exclusion criteria

Exclusion criteria: • Children who received systemic corticosteroids (any preparation, any dose, any route) for more than 3 weeks in preceding 6 months • Immunosuppressed states including diabetes mellitus, chronic renal failure, chronic liver failure and others • Children with rickets, skeletal chest deformity, bronchopulmonary dysplasia, coexisting primary parenchymal pulmonary disease (e.g., cystic fibrosis, bronchiectasis), known case of vitamin ?D deficiency or parathyroid disease, and those received vitamin D or calcium supplements in past 3 months. • Underlying disease (e.g., lupus erythematosus, IgA nephropathy, amyloidosis) • Evidence of steroid toxicity: Cataract, glaucoma, body mass index >30 or height

Design outcomes

Primary

MeasureTime frame
a)Percentage change in lung function parameters measured by forced oscillation technique (i.e Resistance (R5, R20), reactance (X5, X20), AXTimepoint: At baseline, 1 month, 2 month, 3 month and at 6 month

Secondary

MeasureTime frame
a) Level of asthma control (Asthma control test and GINA assessment) b) Number of asthma exacerbations c) Use of systemic steroids d) Number of emergency visits e) Number of hospitalizations f) Vitamin D3 levels at 3 months, adverse effect of Vitamin D g) Change in serum IgE from baseline to end of follow-up h) Change in R5, X5 from baseline to end of therapy i) Change in R5, X5 between follow-up visits j) Corelation with spirometry parameters FEV1, FVC k) Change in asthma control test score between follow-up visits l) Therapy associated adverse events including, impaired glucose metabolism, obesity, cushingoid habitus, cataract, glaucoma, hirsutism, growth abnormality Timepoint: 0, 1,2,3,6 months

Countries

India

Contacts

Public ContactSachin Singh

AIIMS Rajkot

dr.sachinaiimsrajkot@gmail.com8859150624

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026