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Comparison of fluticasone/vilanterol vs fluticasone/salmeterol in stable copd patients

COMPARISON OF SAFETY AND EFFICACY OF FLUTICASONE FUROATE/VILANTEROL VERSUS FLUTICASONE FUROATE/SALMETEROL IN THE TREATMENT OF MODERATE STABLE COPD PATIENTS - A RANDOMIZED CONTROLLED TRIAL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/02/039895
Enrollment
60
Registered
2022-02-01
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Health Condition 1: J40-J47- Chronic lower respiratory diseases

Interventions

Intervention1: fluticasone furoate/vilanterol: fluticasone furoate 100 mcg/vilanterol 25 mcg powder for inhalation OD for 3 months. Control Intervention1: Fluticasone furoate/salmeterol: fluticasone f

Sponsors

SRM college of pharmacy
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: subjects with clinical history of moderate copd in accordance with the following definition by the european respiratory society. subjects with measured FEV1/FVC ratio of 0.70 at screening. subjects with measured FEVI 70% of predicted normal values. patient willing to participate in the study and providing informed consent.

Exclusion criteria

Exclusion criteria: patients with 70 years of age and women of reproductive age (15-45 years). patients with symptoms of acute exacerbation. patients with uncontrolled diabetes mellitus and hypertension. patients on immunosuppressive drugs. patients with known trigger factors of asthma and malignancy.

Design outcomes

Primary

MeasureTime frame
spirometry change complete blood countTimepoint: basal,14th day, 28th day,2nd month,3rd month.

Secondary

MeasureTime frame
ST.George respiratory questionnaire.Timepoint: Baseline, 3rd month.

Countries

India

Contacts

Public ContactVidhya shree

SRM College of Pharmacy, SRM Institute of Science and Technology

priyadha@srmist.edu.in9787402050

Outcome results

None listed

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