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NCT07372573Not yet recruiting

Pressurized Meter Dose Inhaler V/S Dry Powder Inhaler

Effectivenes of Pressurized Meter Dose Inhaler (PMDI) Versus Dry Powder Inhaler (DPI) in Delivering Inhaled Corticosteroid and Long Acting Beta Agonist Among Patients With Uncontrolled Asthma in a Tertiary Care Hospital.

Source: ClinicalTrials.gov · Last updated 28 Jan 2026

Brief summary (registry, in English)

This study compares two commonly used inhalation devices in asthma management. It focuses on evaluating how effectively PMDIs and DPIs deliver the same combination of inhaled corticosteroids and long-acting beta agonists in patients whose asthma remains poorly controlled despite treatment. The study is conducted in a tertiary care hospital setting, emphasizing real-world clinical practice and aiming to determine whether device choice influences asthma control outcomes.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
210 (estimated)
First submitted
19 Jan 2026
Start date
1 Feb 2026
Primary completion date
31 Jul 2026
Lead sponsor
University of Health Sciences Lahore
Diseases
Asthma
NCT number
NCT07372573

What you commit to

  • Study type: Interventional
  • Planned participants: 210
  • From 1 Feb 2026 to the primary completion date, 31 Jul 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Patients with Hypersensitivity Pneumonitis
  • Patients with coexistent Interstitial Lung Disease (ILD) (confirmed on spirometry)
  • Patients with coexistent cardiac asthma secondary to heart failure (diagnosed on echocardiography)

Lab values

  • Patients with coexistent fungal sensitization (confirmed with peripheral eosinophil count and serum IgE)
  • Patients with coexistent Allergic Bronchopulmonary Aspergillosis (ABPA) (confirmed with HRCT and serum IgE)

Other

  • Patients with coexistent COPD (confirmed on spirometry)

Who the study is looking for

  • Age 14 to 60 years
  • Both genders
  • All patients with symptoms of uncontrolled asthma

Age in the registry: 14 years to 60 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Services Hospital Lahore
Coordinator of this site? Confirm its status
LahorePakistanUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.