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Evaluation of phytopharmaceuticals to improve the prognosis of Covid-19 disease in Togo.

Evaluation of phytopharmaceuticals to improve the prognosis of Covid-19 disease in Togo.

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
PACTR
Registry ID
PACTR202009483194545
Enrollment
250
Registered
2020-09-21
Start date
2020-10-15
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

SARS-CoV-2 Infection

Interventions

IMMUTOP
IMMUNITUM
SECURE
BIOCIRE
Hydroxychloroquine and Azithromycine

Sponsors

University of Lome
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Patients over 18 years of age. - Infected with a Covid-19 infection confirmed by a specific PCR. - Hospitalized. - Fever or cough - No signs of respiratory distress - Naïve of specific treatment for Covid-19. - Informed consent signed by the patient.

Exclusion criteria

Exclusion criteria: - Renal insufficiency (eGFR 3 times normal - Cirrhosis (stage = Child-Pugh B). - Pregnancy or breastfeeding. - Dementia or any other condition that does not allow for informed consent. - Any reason that, at the discretion of the investigator, would compromise patient safety and cooperation in the trial.

Design outcomes

Primary

MeasureTime frame
Proportion of patients with undetectable viral load

Secondary

MeasureTime frame
Proportion of patients with clinical improvement on the 7-point ordinal scale ;Proportion of patients who died or were affected by respiratory distress syndrome;Prevalence of grade 3 and 4 adverse events in each treatment group ;Proportion of patient cured

Countries

Togo

Contacts

Public ContactKOKOU Kouami

Director of the Master Research Program University lecturer of ecology and forest natural resources management

kokoukouami@wascal-togo.org+22890020411

Outcome results

None listed

Source: PACTR (via WHO ICTRP) · Data processed: Aug 9, 2026