albuterol has been researched along with Late Onset Diseases in 1 studies
Albuterol: A short-acting beta-2 adrenergic agonist that is primarily used as a bronchodilator agent to treat ASTHMA. Albuterol is prepared as a racemic mixture of R(-) and S(+) stereoisomers. The stereospecific preparation of R(-) isomer of albuterol is referred to as levalbuterol.
albuterol : A member of the class of phenylethanolamines that is 4-(2-amino-1-hydroxyethyl)-2-(hydroxymethyl)phenol having a tert-butyl group attached to the nirogen atom. It acts as a beta-adrenergic agonist used in the treatment of asthma and chronic obstructive pulmonary disease (COPD).
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 1 (100.00) | 2.80 |
Authors | Studies |
---|---|
Koeberl, DD | 1 |
Case, LE | 1 |
Desai, A | 1 |
Smith, EC | 1 |
Walters, C | 1 |
Han, SO | 1 |
Thurberg, BL | 1 |
Young, SP | 1 |
Bali, D | 1 |
Kishnani, PS | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Phase 1/2 Double-Blind Study of the Safety and Efficacy of Albuterol on Motor Function in Individuals With Late-onset Pompe Disease Receiving Enzyme Replacement Therapy[NCT01885936] | Phase 1/Phase 2 | 16 participants (Actual) | Interventional | 2013-06-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
All participants who experienced adverse events. (NCT01885936)
Timeframe: 52 weeks
Intervention | Participants (Count of Participants) |
---|---|
Albuterol | 5 |
Placebo Comparator | 5 |
The distance covered over a time of 6 minutes is used as the outcome by which to compare changes in performance capacity. Assessed by physical therapist. (NCT01885936)
Timeframe: Baseline, Week 6, and Week 52
Intervention | meters (Mean) | |
---|---|---|
Change at 6 Weeks | Change at 52 Weeks | |
Albuterol | 24.0 | 43.6 |
Placebo Comparator | 32.0 | 13.6 |
FVC (forced vital capacity) is the amount of air which can be forcibly exhaled from the lungs after taking the deepest breath possible. (NCT01885936)
Timeframe: Baseline, Week 30, and Week 52
Intervention | Percent of predicted FVC (Mean) | |
---|---|---|
Change at 30 Weeks | Change at 52 Weeks | |
Albuterol | -0.2 | -1.3 |
Placebo Comparator | 0.4 | 3.0 |
1 trial available for albuterol and Late Onset Diseases
Article | Year |
---|---|
Improved muscle function in a phase I/II clinical trial of albuterol in Pompe disease.
Topics: Adult; Albuterol; Double-Blind Method; Enzyme Replacement Therapy; Female; Forced Expiratory Volume; | 2020 |