Covid19 Clinical Trial
— PHYTCOVID-19Official title:
Evaluation de l'efficacité et de la tolérance de Quinquina et d'un phytomédicament " ACAR " en Comparaison Avec l'Hydroxychloroquine Chez Des Adultes Malades de Covid-19 Sans symptômes
Our previous work on plants has indicated significant antimalarial and antiviral activities.
Of these plants, two recipes are proposed for evaluation for COVID-19. It is Cinchona, an
antimalarial and a combination of 4 plants with antiviral, antimalarial, antitussive and
anti-inflammatory properties.
The phase II clinical trial, with three arms and at a rate of 77 patients per arm, received
the approval of the National Committee for Ethics and Health Research. This is a
non-inferiority test aimed at comparing the therapeutic impact in "add on" to Azithromycin,
phytomedicines versus Hydroxychloroquine in asymptomatic COVID-19 patients.
After 10 days of treatment, viral clearance and symptom progression will be assessed on days
3, 6 and 14. Clinical, paraclinical and laboratory tests will be performed throughout the
3-month trial. Ethical and deontological considerations will be applied
Status | Enrolling by invitation |
Enrollment | 231 |
Est. completion date | September 30, 2020 |
Est. primary completion date | August 30, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Eligible patients are adults with COVID-19 confirmed by a positive PCR (Polymerase Chain Reaction) test and without symptoms Exclusion Criteria: - any patient hypersensitive to hydroxychloroquine or under traditional herbal treatment in the two weeks preceding inclusion, - any patient with other acute or chronic illnesses such as heart failure, arterial hypertension, renal failure, hepatocellular failure, tuberculosis or unable to take the oral treatment; - any patient for whom one of the treatments under study is contraindicated according to the doctor's opinion. - pregnant women, - severe neurological manifestations |
Country | Name | City | State |
---|---|---|---|
Guinea | Support Centers of Donka, Kenien and Gbessia | Conakry |
Lead Sponsor | Collaborator |
---|---|
Institute for Research and Development of Medicinal and Food Plants of Guinea |
Guinea,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Virologic clearance of throat swabs or lower respiratory tract secretions | Virologic clearance from admission to discharge at days 3, 6 and 14 | day 3 to day 14 | |
Secondary | COVID-19 symptoms development | number of patients who developed fever, cough, and any other clinical sign typical of the disease | day 1 to day 14 | |
Secondary | Adverse effects | number of participants who developed treatment-related adverse effects | day 1 to day 14 | |
Secondary | Worsened condition | number of patients whose condition worsened on D14 | day 1 to day 14 |
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