clenbuterol has been researched along with Prosthesis Durability in 1 studies
Clenbuterol: A substituted phenylaminoethanol that has beta-2 adrenomimetic properties at very low doses. It is used as a bronchodilator in asthma.
clenbuterol : A substituted aniline that is 2,6-dichloroaniline in which the hydrogen at position 4 has been replaced by a 2-(tert-butylamino)-1-hydroxyethyl group.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 1 (100.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Birks, EJ | 1 |
Tansley, PD | 1 |
Hardy, J | 1 |
George, RS | 1 |
Bowles, CT | 1 |
Burke, M | 1 |
Banner, NR | 1 |
Khaghani, A | 1 |
Yacoub, MH | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
Harefield Recovery Protocol Study (HARPS): A Nonrandomized, Open Label, Multicenter Evaluation of Potential Recovery of Heart Function in Patients With Refractory Chronic Heart Failure by Treatment With Combination of Left Ventricular Assist Device (LVAD)[NCT00585546] | Phase 1 | 18 participants (Actual) | Interventional | 2007-07-31 | Terminated (stopped due to No longer could obtain clenbuterol) | ||
Interleukin-1 Receptor Antagonist for the Treatment of Heart Failure in Patients With Left Ventricular Assist Devices[NCT02547766] | Phase 1/Phase 2 | 10 participants (Actual) | Interventional | 2015-04-30 | Completed | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
(NCT00585546)
Timeframe: 18 months after explantation
Intervention | absolute change in ejection fraction (Number) |
---|---|
LVAD and Clenbuterol | -.09 |
(NCT00585546)
Timeframe: up to 16 months, variable based on length of time receiveing clenbuterol
Intervention | ejection fraction (Mean) |
---|---|
LVAD and Clenbuterol | 0.16 |
Scale 0 - 105 (0- 5 on 21 items) where 0 means heart failure has not limited daily life at all and high scores mean that daily functions are greatly limited. (NCT00585546)
Timeframe: 6 months following LVAD implantation
Intervention | units on a scale (Mean) |
---|---|
LVAD and Clenbuterol | 28.3 |
(NCT00585546)
Timeframe: Up to 16 months after LVAD implantation (12 months after beginning clenbuterol)
Intervention | Participants (Count of Participants) |
---|---|
LVAD and Clenbuterol | 13 |
(NCT00585546)
Timeframe: One year after LVAD explant or until transplant or death (if not explanted)
Intervention | percentage of participants (Number) |
---|---|
LVAD and Clenbuterol | 5.6 |
(NCT00585546)
Timeframe: Maximum 12 months after LVAD implantation
Intervention | Participants (Count of Participants) |
---|---|
LVAD and Clenbuterol | 1 |
Time from LVAD placement to explant for the single participant who achieved explant (NCT00585546)
Timeframe: Time to explant (but not to be followed for more than 16 months)
Intervention | weeks (Number) |
---|---|
LVAD and Clenbuterol | 28 |
(NCT00585546)
Timeframe: baseline to week 8 post clenbuterol
Intervention | percent change (Mean) | |
---|---|---|
creatinine from baseline to week 8 of clenbuterol | AST from baseline to week 8 on clenbuterol | |
LVAD and Clenbuterol | -15.8 | 15.6 |
(NCT00585546)
Timeframe: Up to 8 weeks after LVAD implantation
Intervention | percent change (Mean) | |
---|---|---|
Creatinine | aspartate transaminase (AST) | |
LVAD and Clenbuterol | 17.2 | 25 |
Scale 0 - 100 where 0 is worst possible health state and 100 is perfect health. (NCT00585546)
Timeframe: 1 year following LVAD implantation
Intervention | units on a scale (Mean) | |
---|---|---|
6 months post implant | 12 months post implant | |
LVAD and Clenbuterol | 46 | 51 |
The primary endpoint was a reduction in inflammatory markers, specifically C-reactive protein (CRP). (NCT02547766)
Timeframe: 6 months post treatment
Intervention | mg/dL (Median) | ||
---|---|---|---|
Prior to Anakinra | After Anakinra | At 6 months | |
Anakinra Arm | 2.5 | 0.6 | 0.6 |
Secondary endpoints included the measure of additional inflammatory markers, including neutrophil count. (NCT02547766)
Timeframe: 6 months post treatment
Intervention | 10^3 cells/µL (Median) | ||
---|---|---|---|
Prior to Anakinra | After Anakinra | At 6 months | |
Anakinra Arm | 6.4 | 5.0 | 4.4 |
Secondary endpoints included the measure of additional inflammatory markers, including TNFalpha. (NCT02547766)
Timeframe: 6 months post treatment
Intervention | pg/mL (Median) | ||
---|---|---|---|
Prior to Anakinra | After Anakinra | At 6 months | |
Anakinra Arm | 4 | 9 | 4 |
Clinical efficacy was a secondary endpoint that was measured using ejection fraction (EF) (NCT02547766)
Timeframe: 6 months post treatment
Intervention | percentage of blood leaving heart (Median) | ||
---|---|---|---|
Prior to Anakinra | After Anakinra | At 6 months | |
Anakinra Arm | 15 | 15 | 25 |
1 trial available for clenbuterol and Prosthesis Durability
Article | Year |
---|---|
Left ventricular assist device and drug therapy for the reversal of heart failure.
Topics: Adolescent; Adrenergic beta-2 Receptor Agonists; Adrenergic beta-Agonists; Adult; Blood Pressure; Ca | 2006 |
Left ventricular assist device and drug therapy for the reversal of heart failure.
Topics: Adolescent; Adrenergic beta-2 Receptor Agonists; Adrenergic beta-Agonists; Adult; Blood Pressure; Ca | 2006 |
Left ventricular assist device and drug therapy for the reversal of heart failure.
Topics: Adolescent; Adrenergic beta-2 Receptor Agonists; Adrenergic beta-Agonists; Adult; Blood Pressure; Ca | 2006 |
Left ventricular assist device and drug therapy for the reversal of heart failure.
Topics: Adolescent; Adrenergic beta-2 Receptor Agonists; Adrenergic beta-Agonists; Adult; Blood Pressure; Ca | 2006 |