Evaluating the Efficacy of Artesunate in Adults With Mild Symptoms of COVID-19
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ClinicalTrials.gov Identifier: NCT04387240 |
Recruitment Status :
Withdrawn
(did not get enough fund and IRB request)
First Posted : May 13, 2020
Last Update Posted : May 2, 2022
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Coronavirus disease (COVID-19) is an infectious disease caused by a newly discovered coronavirus.
At this time, there are no specific vaccines or treatments for COVID-19. However, there are many ongoing clinical trials evaluating potential treatments Drugs used to treat malaria infection has shown to be beneficial for many other diseases, including viral infections.
In this Clinical trial, Investigators will evaluate the effect of Artemisinin / Artesunate on morbidity of COVID-19 patients in decreasing the course of the disease and viral load in symptomatic stable positive swab COVID-19 patients. Investigators are hypothesizing that due to the antiviral properties of this drug it will help as a treatment for the COVID -19 patients. In improving their condition and clearing the virus load,
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Covid 19 Positive Corona Virus Infection | Drug: Artemisinin / Artesunate Other: placebo | Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 0 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Intervention Model Description: | double blind controlled trial |
Masking: | Triple (Participant, Care Provider, Investigator) |
Masking Description: | the pharmacy will do the randomization of the labeled drug and placebo |
Primary Purpose: | Treatment |
Official Title: | Evaluating the Efficacy of Artesunate in Adults With Mild Symptoms of COVID-19 |
Estimated Study Start Date : | January 2022 |
Estimated Primary Completion Date : | September 2022 |
Estimated Study Completion Date : | December 2022 |

Arm | Intervention/treatment |
---|---|
Experimental: intervention group
this group will receive the Artemisinin / Artesunate 100mg once daily for 5 days
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Drug: Artemisinin / Artesunate
testing the drug capabilities in reducing the shedding and causing the testing for covid 19 to become negative |
Placebo Comparator: placibo
this group will receive a placebo of the same shape and picture of the study drug
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Other: placebo
placebo or sham drug will be given to the second arm |
- length of stay in hospital [ Time Frame: within the first 6 days intervention ]absence of the virus shedding evidenced by negative swabs
- number of ICU admission [ Time Frame: 14 days ]reduction of morbidity and mortality
- resolution of symptoms [ Time Frame: 6 days - 10 day ]finding the time that the symptoms disappear

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 18 Years to 60 Years (Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Adult patient age more than 18 and less than 60 years
- Symptomatic , positive swab covid-19 patients
- Patients who have mild to moderate symptoms
- Patients who have no risk factors like
- Patients who is not on other medications rather those on supportive care
Exclusion Criteria:
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· Patients who have sever disease- shortness of breath, sick patients or admitted in ICU
- Patients who are receiving ventilation supports
- High risk group like :- age more than 60 years, chronic heart diseases, chronic lungs diseases, diabetes, immunocompromised diseases or on immune suppression medications or pregnant women
- Patients who are on other medications which used as treatment for covid 19

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04387240
Saudi Arabia | |
Princess Nourah Bint Abdulrahman Univeristy | |
Riyadh, Central, Saudi Arabia, 11552 |
Principal Investigator: | Osama Kentab, MD | Princess Nourah Bint Abdulrahman University |
Responsible Party: | osama y kentab, Clinical Associate Professor of Emergency Medicine, Princess Nourah Bint Abdulrahman University |
ClinicalTrials.gov Identifier: | NCT04387240 |
Other Study ID Numbers: |
20-0192 |
First Posted: | May 13, 2020 Key Record Dates |
Last Update Posted: | May 2, 2022 |
Last Verified: | April 2022 |
Individual Participant Data (IPD) Sharing Statement: | |
Plan to Share IPD: | No |
Studies a U.S. FDA-regulated Drug Product: | No |
Studies a U.S. FDA-regulated Device Product: | No |
artemisinin Artesunate |
COVID-19 Artesunate Coronavirus Infections Respiratory Tract Infections Infections Pneumonia, Viral Pneumonia Virus Diseases Coronaviridae Infections Nidovirales Infections RNA Virus Infections Lung Diseases |
Respiratory Tract Diseases Artemisinins Artemisinin Antimalarials Antiprotozoal Agents Antiparasitic Agents Anti-Infective Agents Antineoplastic Agents Antiviral Agents Schistosomicides Antiplatyhelmintic Agents Anthelmintics |