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Trial - EUCTR2020-001704-42-ES


Column Value
Trial registration number EUCTR2020-001704-42-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

IDIVAL - Mar García Sáiz

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

mmar.garcia@scsalud.es

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

2020-05-21

Recruitment status
Last imported at : Sept. 22, 2023, midnight
Source : EU Clinical Trials Register

Terminated

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

Parallel

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

Blind 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

Prevention

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

1) Healthcare professional aged between 18 and 65 (inclusive) at the time of the first selection visit. 2) Must provide a signed written informed consent and agree to adhere to the study protocol. 3) Active work in high exposure areas during the last two weeks and during the following weeks. 1) Profesional sanitario con edad comprendida entre los 18 y los 65 años (inclusive) en el momento de la primera visita de selección. 2) Deben proporcionar un consentimiento informado por escrito firmado y aceptar cumplir con el protocolo del estudio. 3) Trabajo activo en áreas de alta exposición durante las dos últimas semanas y durante las siguientes semanas.

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

1) Previous infection by SARS CoV2 (positive coronavirus PCR or positive IgG serology with negative SARS Cov2 PCR and absence of symptoms). 2) Current treatment with HCQ or chloroquine 3) Contraindication for taking HCQ (known epilepsy, porphyria, recent ischemic heart disease). 4) Previous or current treatment with tamoxifen or raloxifene. 5) Previous eye disease, especially maculopathy. 6) Known heart failure (Grade III-IV of the New York Heart Association classification) or prolonged QTc. 7) Any type of cancer (except basal cell) in the last 5 years. 6) Refusal to give informed consent. 8) Signs of any other untreated, unstable or clinically significant immunological, endocrine, hematological, gastrointestinal, neurological, neoplasic or psychiatric disease. 9) Positive antibodies to human immunodeficiency virus . 10) Significant kidney or liver disease. 11) Pregnancy or lactation 12) Hypersensitivity or allergy to HCQ, or any contraindication in Summary of Product Characteristics to HCQ intake. 1) Infección previa por SARS CoV2 (PCR coronavirus positiva o Serología IgG positiva con PCR SARS Cov2 negativa y ausencia de sintomatología). 2) Tratamiento actual con HCQ o cloroquina. 3) Contraindicación para la toma de HCQ (epilepsia conocida, porfiria, cardiopatía isquémica reciente). 4) Tratamiento previo o actual con tamoxifeno o raloxifeno. 5) Enfermedad ocular previa, especialmente maculopatía. 6) Insuficiencia cardíaca conocida (Grado III a IV de la clasificación de la Asociación de Cardiología de Nueva York [New York Heart Association) o QTc prolongado. 7) Cualquier tipo de cáncer (excepto basocelular) en los últimos 5 años. 6) Negativa a dar el consentimiento informado. 8) Indicios de cualquier otra enfermedad inmunológica, endocrina, hematológica, gastrointestinal, neurológica, neoplásica o psiquiátrica inestable o clínicamente significativa sin tratar. 9) Anticuerpos positivos para el virus de la inmunodeficiencia humana. 10) Enfermedad renal o hepática significativas. 11) Embarazo o lactancia, 12) Hipersensibilidad o alergia a la HCQ, o cualquier contraindicación en ficha técnica a la toma de HCQ

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

IDIVAL Instituto de Investigación Sanitaria Valdecilla

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

65

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

Health workers

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

N/A

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

450

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

- Number of healthcare professionals with symptomatic or asymptomatic SARS-CoV2 infection. - Severity of the infection. - Número de profesionales sanitarios con infección sintomática o asintomática por SARS-CoV2. - Gravedad de la infección.

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

Declared number of arm (3.0) differs from found arms (2.0)

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": 607, "treatment_name": "Hydroxychloroquine", "treatment_type": "Antimalarials", "pharmacological_treatment": "Pharmacological treatment"}, {"arm_notes": "", "treatment_id": 2187, "treatment_name": "Placebo", "treatment_type": "Placebo", "pharmacological_treatment": "Placebo"}]