albuterol has been researched along with Hematologic Malignancies 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 | 1 (100.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Barisione, G | 1 |
Bacigalupo, A | 1 |
Crimi, E | 1 |
Brusasco, V | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Acute Bronchodilator Responsiveness in Obliterative Bronchiolitis (OB) Following Hematopoietic Stem Cell Transplantation[NCT01112241] | Phase 4 | 17 participants (Actual) | Interventional | 2010-04-30 | Completed | ||
Predictive Value of Within-breath Respiratory Input Impedance in the Early Diagnosis of Obliterative Bronchiolitis After Allogeneic Hematopoietic Stem Cell Transplantation[NCT01255449] | 26 participants (Actual) | Interventional | 2010-12-31 | Completed | |||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Following albuterol plus tiotropium inhalation, FEV1 increments ≥0.20 liters (L) as compared to baseline, in an individual subject, were considered as evidence of response to bronchodilators, according to the American Thoracic Society-European Respiratory Society standard criteria [Pellegrino et al. Eur Respir J 2005; 26: 948-968]. They were calculated as follows: [FEV1 (L) after bronchodilators - FEV1 (L) before bronchodilators]. (NCT01112241)
Timeframe: Baseline and 90 min after bronchodilators
Intervention | absolute positive change (liters) (Mean) | |
---|---|---|
Responsives to bronchodilators (n=4) | Unresponsives to bronchodilators (n=13) | |
Albuterol Plus Tiotropium | 0.26 | 0.12 |
Following albuterol plus tiotropium inhalation, FVC increments ≥0.20 liters (L) compared with baseline, in an individual subject, were considered as evidence of response to bronchodilators, according to the American Thoracic Society-European Respiratory Society standard criteria [Pellegrino et al. Eur Respir J 2005; 26: 948-968]. They were calculated as follows: [FVC (L) after bronchodilators - FVC (L) before bronchodilators]. (NCT01112241)
Timeframe: Baseline and 90 min after bronchodilators
Intervention | absolute positive change (liters) (Mean) | |
---|---|---|
Responsives to bronchodilators (n=5) | Unresponsives to bronchodilators (n=12) | |
Albuterol Plus Tiotropium | 0.65 | 0.07 |
Following albuterol plus tiotropium inhalation, FRC decrements ≥0.30 liters (L) as compared to baseline, in an individual subject, were considered as evidence of response to bronchodilators, according to O'Donnell et al. [Eur Respir J 2001; 18: 914-920]. They were calculated as follows: [FRC (L), before bronchodilators - FRC (L) after bronchodilators]. (NCT01112241)
Timeframe: Baseline and 90 min after bronchodilators
Intervention | absolute negative change (liters) (Mean) | |
---|---|---|
Responsives to bronchodilators (n=4) | Unresponsives to bronchodilators (n=13) | |
Albuterol Plus Tiotropium | 0.78 | 0.07 |
Following albuterol plus tiotropium inhalation, RV decrements ≥0.30 liters (L) as compared to baseline, in an individual subject, were considered as evidence of response to bronchodilators, according to O'Donnell et al. [Eur Respir J 2001; 18: 914-920]. They were calculated as follows: [RV (L), before bronchodilators - RV (L) after bronchodilators]. (NCT01112241)
Timeframe: Baseline and 90 min after bronchodilators
Intervention | absolute negative change (liters) (Mean) | |
---|---|---|
Responsives to bronchodilators (n=8) | Unresponsives to bronchodilators (n=9) | |
Albuterol Plus Tiotropium | 0.65 | 0.00 |
Following albuterol plus tiotropium inhalation, FEV1 increments ≥12 per cent as compared to baseline, in an individual subject, were considered as evidence of response to bronchodilators, according to the American Thoracic Society-European Respiratory Society standard criteria [Pellegrino et al. Eur Respir J 2005; 26: 948-968]. They were calculated as follows: [FEV1, expressed in liters (L), after bronchodilators - FEV1 (L) before bronchodilators/FEV1 (L) before bronchodilators x 100]. (NCT01112241)
Timeframe: Baseline and 90 min after bronchodilators
Intervention | per cent positive change (Mean) | |
---|---|---|
Responsives to bronchodilators (n=4) | Unresponsives to bronchodilators (n=13) | |
Albuterol Plus Tiotropium | 14 | 7 |
Following albuterol plus tiotropium inhalation, FVC increments ≥12 per cent as compared to baseline, in an individual subject, were considered as evidence of response to bronchodilators, according to the American Thoracic Society-European Respiratory Society standard criteria [Pellegrino et al. Eur Respir J 2005; 26: 948-968]. They were calculated as follows: [FVC, expressed in liters (L), after bronchodilators - FVC (L) before bronchodilators/FVC (L) before bronchodilators x 100]. (NCT01112241)
Timeframe: Baseline and 90 min after bronchodilators
Intervention | per cent positive change (Mean) | |
---|---|---|
Responsives to bronchodilators (n=5) | Unresponsives to bronchodilators (n=12) | |
Albuterol Plus Tiotropium | 24 | 2 |
Following albuterol plus tiotropium inhalation, FRC decrements ≥10 per cent as compared to baseline, in an individual subject, were considered as evidence of response to bronchodilators, according to O'Donnell et al. [Eur Respir J 2001; 18: 914-920]. They were calculated as follows: [FRC, expressed in liters (L), before bronchodilators - FRC (L) after bronchodilators/FRC (L) after bronchodilators x 100]. (NCT01112241)
Timeframe: Baseline and 90 min after bronchodilators
Intervention | per cent negative change (Mean) | |
---|---|---|
Responsives to bronchodilators (n=4) | Unresponsives to bronchodilators (n=13) | |
Albuterol Plus Tiotropium | 16 | 2 |
Following albuterol plus tiotropium inhalation, V'max increments ≥40 per cent as compared to baseline, in an individual subject, were considered as evidence of response to bronchodilators, according to Pellegrino et al. [Chest 1998; 114:1607-1612]. They were calculated as follows: [V'max, expressed in liters.second-1 (L.s-1), after bronchodilators - V'max (L.s-1) before bronchodilators/V'max (L.s-1) before bronchodilators x 100]. (NCT01112241)
Timeframe: Baseline and 90 min after bronchodilators
Intervention | per cent positive change (Mean) | |
---|---|---|
Responsives to bronchodilators (n=4) | Unresponsives to bronchodilators (n=13) | |
Albuterol Plus Tiotropium | 66 | 14 |
Following albuterol plus tiotropium inhalation, V'part increments ≥40 per cent as compared to baseline, in an individual subject, were considered as evidence of response to bronchodilators, according to Pellegrino et al. [Chest 1998; 114:1607-1612]. They were calculated as follows: [V'part, expressed in liters.second-1 (L.s-1), after bronchodilators - V'part (L.s-1) before bronchodilators/V'part (L.s-1) before bronchodilators x 100]. (NCT01112241)
Timeframe: Baseline and 90 min after bronchodilators
Intervention | per cent positive change (Mean) | |
---|---|---|
Responsives to bronchodilators (n=9) | Unresponsives to bronchodilators (n=8) | |
Albuterol Plus Tiotropium | 59 | 17 |
Following albuterol plus tiotropium inhalation, RV decrements ≥10 per cent as compared to baseline, in an individual subject, were considered as evidence of response to bronchodilators, according to O'Donnell et al. [Eur Respir J 2001; 18: 914-920]. They were calculated as follows: [RV, expressed in liters (L), before bronchodilators - RV (L) after bronchodilators/RV (L) after bronchodilators x 100]. (NCT01112241)
Timeframe: Baseline and 90 min after bronchodilators
Intervention | per cent negative change (Mean) | |
---|---|---|
Responsives to bronchodilators (n=8) | Unresponsives to bronchodilators (n=9) | |
Albuterol Plus Tiotropium | 19 | 0 |
We studied 26 subjects, 2 weeks before and 2 months after HSCT. Within-breath respiratory system conductance (Grs) at 5, 11 and 19 Hz was measured by forced oscillation technique (FOT) at functional residual capacity (FRC) and total lung capacity (TLC) (NCT01255449)
Timeframe: 2 weeks before and 2 months after HSCT
Intervention | 1/cmH2O*s (Mean) |
---|---|
Airway Distensibility With Lung Inflation After HSCT | 0.07 |
Changes in lung tissue density were measured by quantitative computed tomography(CT) scan 2 weeks before and 2 months after HSCT (NCT01255449)
Timeframe: Before and 2 months after HSCT
Intervention | g/mL (Mean) |
---|---|
Post-HSCT Changes in Lung Tissue Density | 0.03 |
1 other study available for albuterol and Hematologic Malignancies
Article | Year |
---|---|
Acute bronchodilator responsiveness in bronchiolitis obliterans syndrome following hematopoietic stem cell transplantation.
Topics: Administration, Inhalation; Adult; Albuterol; Bronchiolitis Obliterans; Bronchodilator Agents; Drug | 2011 |
Acute bronchodilator responsiveness in bronchiolitis obliterans syndrome following hematopoietic stem cell transplantation.
Topics: Administration, Inhalation; Adult; Albuterol; Bronchiolitis Obliterans; Bronchodilator Agents; Drug | 2011 |
Acute bronchodilator responsiveness in bronchiolitis obliterans syndrome following hematopoietic stem cell transplantation.
Topics: Administration, Inhalation; Adult; Albuterol; Bronchiolitis Obliterans; Bronchodilator Agents; Drug | 2011 |
Acute bronchodilator responsiveness in bronchiolitis obliterans syndrome following hematopoietic stem cell transplantation.
Topics: Administration, Inhalation; Adult; Albuterol; Bronchiolitis Obliterans; Bronchodilator Agents; Drug | 2011 |