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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04584567
Other study ID # UR17DN05
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date November 20, 2020
Est. completion date November 1, 2021

Study information

Verified date November 2021
Source General Administration of Military Health, Tunisia
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Given the urgency of having guidelines for the management of COVID-19 in the current epidemic context and the lack of specific pharmacological treatment, Military Health recommends the launch of a multicenter, randomized, double-blind, interventional clinical trial. The aim of this study is to evaluate the efficacy of a combination of two treatments, low-dose doxcycline (100 mg/day) and Zinc (15 mg/day) (dietary supplement) in the primary prevention of COVID-19 infection in health care professionals in Tunisia compared to two control groups.


Recruitment information / eligibility

Status Completed
Enrollment 194
Est. completion date November 1, 2021
Est. primary completion date February 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - No self-medication with study drugs or antivirals - Negative COVID19 diagnosis confirmed by PCR and negative Elisa antibody assay - No signs of COVID19 - Having given consent for the study Exclusion Criteria: Participation in other clinical trials aimed at primary prevention of VIDOC infection19 - Liver failure - Known allergy to the study product - Pregnancy or breastfeeding - Vitamin A and E treatment in progress

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Doxycyclin
daily (100mg)

Locations

Country Name City State
Tunisia Military Hospital of Tunis Tunis Montfleury

Sponsors (2)

Lead Sponsor Collaborator
Hedi Gharsallah Dacima Consulting

Country where clinical trial is conducted

Tunisia, 

Outcome

Type Measure Description Time frame Safety issue
Primary decreasing the number of cases infected with covid 19 Determine if the use of doxyciciline low dose as preventive treatment decrease the number of cases infected with covid 19 in the active arm compared to the placebo arm. Participants for each randomized treatment arm as compared to placebo. WEEK 6
Secondary Measurement of the emergence of clincal symptoms of COVID 19 Comparison of the emergence of clinical symptoms or COVID-19 diagnosis in participants presenting asymptomatically at study entry but identified as seropositive by serology at entry between the randomized treatment arms and comparator arm. WEEK 6
Secondary the seroprevalence of SARS- CoV 2 IgM/IgG positive samples at study entry and study conclusion in all participants receiving DOXY compared to those receiving placebo. Comparison of the rate of SARS-CoV 2 infections as measured by IgM/IgG seroconversion in study participants receiving randomized DOXY versus placebo. WEEK 6
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