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Trial - EUCTR2020-001437-12-ES


Column Value
Trial registration number EUCTR2020-001437-12-ES
Full text link
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

First author
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Fundació Hospital Universitari Vall d'Hebron - Institut de Recerca (VHIR) - Salvador Augustin

Contact
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Not reported

Registration date
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

2020-04-13

Recruitment status
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Recruiting

Study design
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

RCT

Allocation
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Randomized

Design
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Adaptive

Masking
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Open label

Center
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

single-center

Study aim
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Treatment

Inclusion criteria
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

1. Age 18-80 years 2. Severe COVID-19 pneumonia definied as: - Nasnopharyngeal smear SARS-CoV-2 PCR positive - Pulmonary infiltrates by simple X-ray (or other technique) compatible with pneumonia - One or more of the following criteria: o Room air oxygen saturation <= 94% measured by pulse oximeter o Pa:FiO2 (partial pressure O2/fraction of inspired O2) <=300 o Sa:FiO2 (O2 saturation measured by pulse oximeter/ fraction of inspired O2) <=350 3. Informed Consent according to protocol instructions. 1. Edad 18-80 años 2. Neumonía grave COVID-19 definida como: - Frotis nasofaríngeo con PCR positiva para SARS-CoV-2 - Infiltrados pulmonares por Rx simple (u otra técnica) compatibles con neumonía - Uno o más de los siguientes criterios: o Saturación de oxígeno aire ambiente <= 94% medida con pulsioxímetro o Pa:FiO2 (presión parcial O2/fracción de O2 inspirado) <=300 o Sa:FiO2 (saturación de O2 medida con pulsioxímetro/ fracción de O2 inspirado) <=350 3. Consentimiento informado (especificaciones sobre la obtención del mismo desarrolladas en el protocolo)

Exclusion criteria
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

1. GOT/GPT > 5 the institutional ULN 2. Neutrophils < 500 cell/mmc. 3. Petelet < 50.000 cell/mmc. 4. Documented sepsis o pneumonia different from COVID-19. 5. According to clinician criteria, comorbilities with poor prognosis 6. Compliate Diverticulitis or bowel perforation 7. Current skin infection (p.e piodermitis) 8. According to the clinician criteria, any contraindication for using inmunomodulator tretament. 1. AST/ALT con valores superiores a 5 veces los niveles de normalidad. 2. Neutrófilos < 500 cell/mmc. 3. Plaquetas < 50.000 cell/mmc. 4. Sepsis o neumonía documentada por otros patógenos que no sean COVID-19. 5. Presencia de comorbilidad que puede llevar según juicio clínico a mal pronostico 6. Diverticulitis complicada o perforación intestinal 7. Infección cutánea en curso (p.e piodermitis) 8.Cualquier otra contraindicación al uso de tratamiento inmunomodulador individualizada según criterio clínico de equipo asistencial tratante

Number of arms
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

2

Funding
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Fundació Hospital Universitari Vall d'Hebron - Institut de Recerca (VHIR)

Inclusion age min
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

18

Inclusion age max
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

80

Countries
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Spain

Type of patients
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Severe disease at enrollment

Severity scale
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

6: Severe disease at enrollment

Total sample size
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

290

primary outcome
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Mortality at day 28 after treatment initiation (proportion of patient died that day) Mortalidad a los 28 días de inicio del tratamiento (proporción de pacientes muertos a dicho día)

Notes
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Declared number of arm (4.0) differs from found arms (3.0)

Phase
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

Phase 4

Arms
Last imported at : Oct. 26, 2020, 7:26 a.m.
Source : EU Clinical Trials Register

[{"arm_notes": "", "treatment_id": 283, "treatment_name": "Ciclosporin", "treatment_type": "Immunosuppressants", "pharmacological_treatment": "Pharmacological treatment"}, {"arm_notes": "", "treatment_id": 1299, "treatment_name": "Tocilizumab", "treatment_type": "Interleukin inhibitors", "pharmacological_treatment": "Pharmacological treatment"}]