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Assessment of Efficacy and Safety of HCQ and Antibiotics Administrated to Patients COVID19(+)

Assessment of Efficacy and Safety of HCQ and Antibiotics Administrated to Patients COVID19(+), inTunisia

Status
Withdrawn
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04351919
Acronym
COVID+PA
Enrollment
0
Registered
2020-04-17
Start date
2020-05-05
Completion date
2020-07-15
Last updated
2020-08-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients With COVID19

Brief summary

The study will assess the number of patients who become asymptomatic from clinical signs of COVID19 and will assess the efficacy of Hydroxychloroquine (HCQ) and Azithromycine effects on paucisymptomatic patients with ou without co-morbidities

Interventions

DRUGHydroxychloroquine

400mg per day during 10 days

DRUGAzithromycin

500 mg per day during 5 days

Sponsors

Eshmoun Clinical Research Center
CollaboratorNETWORK
Dacima Consulting
CollaboratorOTHER
Abderrahmane Mami Hospital
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

open, interventional, multicentric study

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* confirmed COVID19 (+) * Qt\<500ms * no severity criteria * pauci-symptomatique patients * signed consent form

Exclusion criteria

* no confirmed patient COVID19 * severity criteria * known allegies to macrolides and HCQ * Treated with HCQ within 1 month prior to inclusion * hepatitis insufficiency * Renal insufficiency * treatment no indicated with azithro and HCQ * hypovolemia * complete brach block * retinopathia * psoriasis * pregnancy or breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
improvment or healing of clinical signsat the end of the study treatment - 1 month after inclusionno respiratory infectious signs
Evolution of clinical signsat the end of the study treatment - 1 month after inclusionLow respiratory signs with severity criteria

Countries

Tunisia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026