Efficacy and Safety of Mucoadhesive Sustained Release Mucodentol in Comparison With Hydroxychloroquine to Prevent COVID-19
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- STATUS
- Recruiting
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- participants needed
- 180
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- sponsor
- Baqiyatallah Medical Sciences University
Summary
180 people from the medical staff and high-risk people in Baqiyatallah Hospital, who are in
close contact with patients, will enter the study. Participants will be divided into two
intervention groups and one control group. The control group will use the full protective
equipment assigned to the treatment staff. In addition to protective equipment, the first
intervention team will receive a daily diet of 200 mg
At the beginning of the treatment, qualified people will participate in the study while recording demographic and clinical information, PCR test will be performed, and if they have negative PCR, they will be in one of the 3 study groups. During the study, if the symptoms of the disease occur in each of the participants, the test will be taken again. If the test is positive, the person will withdraw from the study, and the patient's information will be recorded. Finally, the people present in the study will be tested for PCR, and the results of the disease and the side effects of the drugs will be compared.
Details
Condition | Covid 19 |
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Age | 18years - 100years |
Treatment |
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Clinical Study Identifier | NCT04466280 |
Sponsor | Baqiyatallah Medical Sciences University |
Last Modified on | 19 February 2024 |
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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