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Assessment of patient satisfaction, ease of training and clinical effectiveness of ICS-LABA combinations (in asthma patients) delivered through Ciphaler

Assessment of patient satisfaction ease of training and clinical effectiveness of ICS-LABA combinations delivered through Ciphaler A real world observational study in patients with asthma CONTROL STUDY

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/10/096147
Enrollment
2500
Registered
2025-10-16
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: J45- Asthma

Interventions

Intervention1: Nil: Nil

Sponsors

Cipla Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1 Either gender, of age 18 years or above, with documented diagnosis of Asthma (as per GINA 2025) 2 Prescribed treatment with ICS-LABA delivered through the Ciphaler based on investigator discretion 3 Willing for follow-up at scheduled visit as per protocol 4 A voluntarily given written, signed, dated informed consent from participants and/or legally acceptable representative

Exclusion criteria

Exclusion criteria: 1 Hypersensitivity to the study drug or any of its components 2 Life-threatening or unstable respiratory disease, including lower respiratory tract infection, within the past 4 weeks from screening 3 Acute episodes of asthma requiring systemic corticosteroids, emergency care or hospitalization in the 30 days prior to Baseline visit 4 Chronic pulmonary diseases other than asthma such as COPD, post-tuberculosis lung disease, pulmonary fibrotic disease, or pulmonary arterial hypertension 5 Severe asthma patients receiving biologicals

Design outcomes

Primary

MeasureTime frame
Patient satisfactionTimepoint: 8 weeks

Secondary

MeasureTime frame
1. Ease of training with Ciphaler Timepoint: Baseline;2. Change in ACQ-5 scoreTimepoint: Baseline Week 8;3. Change in ACQ-5 score categories as well controlled (ACQ-5 less than 0.75), partially controlled (ACQ-5 more than 0.75 to less than 1.5), and uncontrolled (ACQ-5 more than 1.5)Timepoint: Baseline week 8;4. Adverse EventTimepoint: Through Study

Countries

India

Contacts

Public ContactVaishali Naik

Cipla Ltd

meena@cipla.com02246185000

Outcome results

None listed

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