Overview

Assessment of the Efficacy and Safety of (HCQ) as a Prophylaxis for COVID19 for Health Professionals

Status:
Withdrawn
Trial end date:
2020-07-15
Target enrollment:
0
Participant gender:
All
Summary
Assessment of the Efficacy and Safety of Hydroxychloroquine (HCQ) Administered as a Prophylaxis for Health Professionals Exposed to COVID19 and Working in Medical Intensive Care Units, in Tunisia. Multicentric, Randomized Comparative Study
Phase:
Phase 3
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Abderrahmane Mami Hospital
Collaborators:
Datametrix
Eshmoun Clinical Research Centre
Treatments:
Hydroxychloroquine
Criteria
Inclusion Criteria:

- Diagnosis of COVID-19 (-)

- Works in a medical intensive care unit exposed to COVID-19 infection

- 18 years old < age < 65 years old

- Having given written consent for their participation in the study.

Exclusion Criteria:

- Diagnosis of COVID-19+

- Retinopathies,

- Hydroxychloroquine or other prophylactic treatments for VIDOC19 within one month prior
to inclusion and throughout the study.

- Hypersensitivity to chloroquine or hydroxychloroquine or 4-aminoquinolines or any of
the other components of this drug,

- Contraindication to prophylactic use of chloroquine, e.g. liver failure, known
epilepsy, creatinine clearance < 30 ml/min.

- Inability to be monitored during the trial period

- Pregnancy and breastfeeding

- Psoriasis