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210507s2020 xx |||||o 00| ||eng c |
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|a (DE-627)WHO007310269
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|a (UBBS_Klinische_Studien_WHO)EUCTR2020-001278-31-ES
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|a (UBBS_Klinische_Studien_WHO)DEXA-COVID19
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|a Efficacy of dexamethasone for treatment of patients affected by COVID-19 with Acute Respiratory Distress Syndrome
|b A comparative, randomised controlled trial for evaluating the efficacy of dexamethasone administration in the treatment of patients affected by COVID-19 with Acute Respiratory Distress Syndrome - DEXA-COVID19
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|c 2020
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|a WHO International Clinical Trials Registry Platform (https://www.who.int/ictrp/en/), First posted: 01-04-2020, Last updated: 2022-11-24
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|a Medical Condition: Acute respiratory distress syndrome (ARDS) in patients affected 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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|a Study Type: Interventional
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|a Phase: Phase 4
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|a Recruitment Status: Authorised-recruitment may be ongoing or finished
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