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A comparative study of Oral doxophylline along with Inhaler therapy and only inhaler therapy in Chronic obstructive pulmonary disease patients.

Comparative study of Oral Doxophylline along with Triple drug therapy versus Triple Drug Therapy in Stable Severe Chronic Obstructive Pulmonary Disease Patients A Randomised control Trial. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/08/071763
Enrollment
76
Registered
2024-08-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-08-19

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

Conditions

Health Condition 1: J449- Chronic obstructive pulmonary disease, unspecified Health Condition 2: J988- Other specified respiratory disorders

Interventions

Intervention1: Tablet Doxophylline: Dosage-650 mg Sustained release Per oral Once daily For 3 months Control Intervention1: Triple drug inhaler therapy Formeterol fumarate, Budesonide, Glycopyronium

Sponsors

SRM medical college hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: At least 6 months of diagnosis of chronic obstructive pulmonary disease, according to GOLD guidelines.(Baseline post bronchodilator forced expiratory volume is less than 50% of predicted value.)

Exclusion criteria

Exclusion criteria: .Patient with bronchial asthma, tuberculosis, lung tumour, bronchiectasis, pneumonia or other diseases that might affect pulmonary function or ventilation. 2. Patients with acute exacerbation of COPD. 3.Patients with congestive heart failure, unstable arrhythmias, chronic hypotension, active peptic ulcer disease, recent myocardial infarction and severe liver/kidney disease. 4.Patients who are unable to take Dry powder/Metered dose inhaler effectively even after adequate training.

Design outcomes

Primary

MeasureTime frame
1.Improvement in symptoms using Chronic obstructive pulmonary disease assessment test scoring scale. 2.Spirometry 3.Six minute walk test Timepoint: 3 months

Secondary

MeasureTime frame
Number of exacerbationsTimepoint: 3 months

Countries

India

Contacts

Public ContactBhagiradhi Thimmapuram

SRM MEDICAL COLLEGE HOSPITAL AND RESEARCH INSTITUTE

subramas1@srmist.edu.in9488507784

Outcome results

None listed

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