Last updated: February 17, 2024
Sponsor: Hat Yai Medical Education Center
Overall Status: Active - Recruiting
Phase
N/A
Condition
Bronchiectasis
Neurologic Disorders
Asthma
Treatment
Placebo
Ipratropium Bromide
Salbutamol plus Ipratropium Bromide
Clinical Study ID
NCT05550402
454554
Ages 18-60 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Asthmatic patients classified by severity Mild (achieved control with using low-doseICS or as-needed ICS-formoterol) or Moderate (achieved controlled with using low-doseICS/LABA or Severe ((achieved controlled with using medium to high dose ICS/LABA)
- Post-bronchodilator (Salbutamol) FEV1/FVC ratio less than 0.75 or below the LowerLimit of Normal (LLN) and Post-bronchodilator (Salbutamol) FEV1 predicted < 80% withor without bronchodilator response
- History of smoking less than 10 pack-years or current smoking
- Patients who able to do spirometry without contraindication
- asthma control was defined by ACQ6 < 1.5
Exclusion
Exclusion Criteria:
- Contraindication for spirometry
- Chest x-ray suggested any chronic lung diseased
- Contraindication for anticholinergic drug
- History of asthma exacerbation within 12 weeks before visit 1
- History of taking LAMA within 6 months before visit 1
Study Design
Total Participants: 60
Treatment Group(s): 4
Primary Treatment: Placebo
Phase:
Study Start date:
February 17, 2024
Estimated Completion Date:
June 30, 2024
Connect with a study center
Hatyai Hospital
Hat Yai, Songkhla 90110
ThailandActive - Recruiting

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