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publishDate:"[2019 TO 2021]"
journalStr:"WHO International Clinical Trials Registry Platform"
topic_facet:"Phase: Phase 2"
topic_facet:"Medical Condition: Acute respiratory distress syndrome caused by Covid-19 MedDRA version: 21.1Level: PTClassification code 10001052Term: Acute respiratory distress syndromeSystem Organ Class: 10038738 - Respiratory, thoracic and mediastinal disorders;Therapeutic area: Diseases [C] - Respiratory Tract Diseases [C08]"
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PubPharm (6)
1
The TRISTARDS trial - ThRombolysIS Therapy for ARDS A study to testwhether different doses of alteplase help people with severe breathingproblems because of COVID 19. : The TRISTARDS trial - ThRombolysIS Therapy for ARDSA Phase IIb/III operationally seamless, open-label, randomised,sequential, parallel-group adaptive study to evaluate the efficacy andsafety of daily intravenous alteplase treatment given up to 5 days on top ofstandard of care (SOC) compared with SOC alone, in patients with acuterespiratory distress syndrome (ARDS) triggered by COVID-19. - -
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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2
The TRISTARDS trial - ThRombolysIS Therapy for ARDS A study to testwhether different doses of alteplase help people with severe breathingproblems because of COVID 19. : The TRISTARDS trial - ThRombolysIS Therapy for ARDSA Phase IIb/III operationally seamless, open-label, randomised,sequential, parallel-group adaptive study to evaluate the efficacy andsafety of daily intravenous alteplase treatment given up to 5 days on top ofstandard of care (SOC) compared with SOC alone, in patients with acuterespiratory distress syndrome (ARDS) triggered by COVID-19. - -
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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3
The TRISTARDS trial - ThRombolysIS Therapy for ARDS A study to test whether different doses of alteplase help people with severe breathing problems because of COVID 19. : The TRISTARDS trial - ThRombolysIS Therapy for ARDSA Phase IIb/III operationally seamless, open-label, randomised, sequential, parallel-group adaptive study to evaluate the efficacy and safety of daily intravenous alteplase treatment given up to 5 days on top of standard of care (SOC) compared with SOC alone, in patients with acute respiratory distress syndrome (ARDS) triggered by COVID-19.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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4
The TRISTARDS trial - ThRombolysIS Therapy for ARDS A study to test whether different doses of alteplase help people with severe breathing problems because of COVID 19. : The TRISTARDS trial - ThRombolysIS Therapy for ARDSA Phase IIb/III operationally seamless, open-label, randomised, sequential, parallel-group adaptive study to evaluate the efficacy and safety of daily intravenous alteplase treatment given up to 5 days on top of standard of care (SOC) compared with SOC alone, in patients with acute respiratory distress syndrome (ARDS) triggered by COVID-19.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
Wird geladen...
5
The TRISTARDS trial - ThRombolysIS Therapy for ARDS A study to test whether different doses of alteplase help people with severe breathing problems because of COVID 19. : The TRISTARDS trial - ThRombolysIS Therapy for ARDSA Phase IIb/III operationally seamless, open-label, randomised, sequential, parallel-group adaptive study to evaluate the efficacy and safety of daily intravenous alteplase treatment given up to 5 days on top of standard of care (SOC) compared with SOC alone, in patients with acute respiratory distress syndrome (ARDS) triggered by COVID-19.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
Wird geladen...
6
The TRISTARDS trial - ThRombolysIS Therapy for ARDS A study to test whether different doses of alteplase help people with severe breathing problems because of COVID 19. : The TRISTARDS trial - ThRombolysIS Therapy for ARDSA Phase IIb/III operationally seamless, open-label, randomised, sequential, parallel-group adaptive study to evaluate the efficacy and safety of daily intravenous alteplase treatment given up to 5 days on top of standard of care (SOC) compared with SOC alone, in patients with acute respiratory distress syndrome (ARDS) triggered by COVID-19.
enthalten in:
WHO International Clinical Trials Registry Platform
| 2021
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1
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Erscheinungsjahr: 2019-2021
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Zeitschrift: WHO International Clinical Trials Registry Platform
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Thema: Phase: Phase 2
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Thema: Medical Condition: Acute respiratory distress syndrome caused by Covid-19 MedDRA version: 21.1Level: PTClassification code 10001052Term: Acute respiratory distress syndromeSystem Organ Class: 10038738 - Respiratory, thoracic and mediastinal disorders;Therapeutic area: Diseases [C] - Respiratory Tract Diseases [C08]
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Zeitschriftentitel
WHO International Clinical Trials Registry Plat...
Thema
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610
Medical Condition: Acute respiratory distress s...
Phase: Phase 2
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Recruitment Status: Authorised-recruitment may ...
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Study Type: Interventional
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2019-2021
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