Effect of the Inhaled Triple Therapies Over the Small Airway in Patients With Chronic Obstructive Pulmonary Disease or Chronic Bronchitis Without Obstruction Secondary to Biomass Exposure: Randomized Controlled Clinical Trial Phase IV

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

This phase IV randomized controlled clinical trial intend to compare the effect of three close standard inhaled triple therapies and one close standard inhaled double therapy on the small airway in patients with Chronic Obstructive Pulmonary Disease (COPD-B) and chronic bronchitis without obstruction (BCNO) exposed to wood smoke. The treatment phase duration is of 3 months. As primary outcome, the resistance change in post-bronchodilatator impulse oscilometry will me measure at 30 minutes, 2 hours, 4 hours, and 24 hours post first dose of the asigned medication, and then at 1 and 3 months of treatment. As secondary outcomes, change in respiratory symptoms and health related quality of life will be assess after 1 and 3 months of treatment.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 35
Maximum Age: 85
Healthy Volunteers: f
View:

• Subject capable of understanding instructions and giving her consent for participation.

• Diagnosis of COPD or chronic bronchitis without obstruction due to biomass smoke exposure:

‣ Diagnosis of COPD according to GOLD guidelines 2023 with: \>100 hours-year of biomass exposure index, and with a post-bronchodilator spirometry FEV1 \> 70% of predicted value.

⁃ Diagnosis of Chronic Bronchitis without obstruction with at least \>100 hours-year of biomass smoke exposure index or more than 10 years of continued exposure to biomass smoke, and with 1) antecedent of chronic bronchitis, and 2) post-bronchodilator spirometry FEV1/FVC \>0.7.

• Able to attend all visits.

• Cooperative patients with adequate understanding and skill in using inhalers, or with caregivers capable of administering medications and filling out a daily symptom diary.

• Stable patients, with no history of exacerbations in the last 4 weeks before inclusion.

Locations
Other Locations
Mexico
Insituto Nacional de Enfermedades Respiratorias Ismael Cosío Villegas
RECRUITING
Mexico City
Contact Information
Primary
Alejandra Ramírez-Venegas, MCs
aleravas@hotmail.com
+52 55 54 87 17 00
Backup
Rogelio Pérez-Padilla, Dr
+52 55 54 87 17 00
Time Frame
Start Date: 2023-11-15
Estimated Completion Date: 2025-01-15
Participants
Target number of participants: 128
Treatments
Experimental: COPD due to biomass exposure
Vilanterol / Umeclidinium 25/62.5 mcg once daily for three months = ANORO® Fluthicasone / Vilanterol / Umeclidinium 100/25/62.5 mcg once daily for three months = TRELEGY® Beclomethasone / Formoterol / Glycopyrronyum 100/6/12.5 mcg; two inhalations twice daily for three months = TRIMBOW® Budesonide / Formoterol / Glycopyrronyum 160/4.8/7.2 mcg; two inhalations twice daily for three months= TRIXEO®
Experimental: Chronic bronchitis without obstruction due to biomass exposure
Vilanterol / Umeclidinium 25/62.5 mcg once daily for three months = ANORO® Fluthicasone / Vilanterol / Umeclidinium 100/25/62.5 mcg once daily for three months = TRELEGY® Beclomethasone / Formoterol / Glycopyrronyum 100/6/12.5 mcg; two inhalations twice daily for three months = TRIMBOW® Budesonide / Formoterol / Glycopyrronyum 160/4.8/7.2 mcg; two inhalations twice daily for three months= TRIXEO®
Sponsors
Leads: National Institute of Respiratory Diseases, Mexico

This content was sourced from clinicaltrials.gov