The Efficacy and Safety of Azovudine in the Treatment of COVID-19

NCT ID: NCT05675761

Last Updated: 2023-01-10

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 500 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2023-01-04
• Study Completion Date: 2024-10-31

Brief Summary

This study is a prospective, multicenter clinical study. It is intended to discuss the efficacy of starting Azovudine treatment as early as possible for all types of patients of COVID-19, the time of remission of specific symptoms, the proportion of patients with severe diseases, oxygen and conditions, and related adverse reactions, so as to understand the efficacy and safety of Azovudine treatment in all types of COVID-19, and provide real world data support for the treatment of the majority of COVID-19 patients.

Detailed Description

1. To evaluate the clinical efficacy of Azovudine in the treatment of mild, moderate and severe COVID-19.

2. To explore the safety and adverse reactions of Azovudine in the whole population of COVID-19.

3. To explore the remission time of clinical symptoms, signs and images of patients with COVID-19 treated with Azovudine.

4. Explore the clinical guiding value of CORMB score.

Conditions

COVID-19; Infections; Morality; Death, Assisted

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: RETROSPECTIVE

Study Groups

Combined bacterial and fungal infection

Combined bacterial and fungal infection

Azorubine

Intervention Type: DRUG

Azovudine tablets, 1mg /tablet, 5 tablets, QD+basic treatment (14 days at most)

No bacterial and fungal infection

No bacterial and fungal infection

Azorubine

Intervention Type: DRUG

Azovudine tablets, 1mg /tablet, 5 tablets, QD+basic treatment (14 days at most)

Interventions

Azorubine

Azovudine tablets, 1mg /tablet, 5 tablets, QD+basic treatment (14 days at most)

Intervention Type: DRUG

Other Intervention Names

basic treatment

Eligibility Criteria

Inclusion Criteria

1. Over 18 years old;

2. Respiratory tract samples (nasopharynx, oropharynx, lower respiratory tract [such as sputum]) collected within 96 hours before enrollment were confirmed to be SARS CoV-2 positive by RT-PCR virus molecular amplification;

3. At least one symptom or sign of COVID-19 (symptoms and signs related to COVID-19, including cough, expectoration, dyspnea, fever, chills, fatigue, muscle soreness, diarrhea, headache, sore throat, nasal congestion, runny nose, etc.);

4. Participants who meet one or more of the following requirements: from the first COVID-19 symptom to the first medication ≤ 5 days;

5. Agree to observe contraceptive measures during the clinical trial;

6. Participants who understand and agree to follow the planned research procedures;

7. Provide follow-up information during the study;

8. Understand the study and be willing to sign the informed consent form.

Exclusion Criteria

1. Those who are known to be allergic to any component of the intervention preparation used in the test;

2. Patients with abnormal liver function test (alanine aminotransferase and /or glutamic oxaloacetic aminotransferase exceed the upper limit of normal value by 3 times, or total bilirubin exceeds the upper limit of normal value by 2 times);

3. Patients with a known history of liver disease (cirrhosis with ChildPugh grade B and C);

4. Congestive heart failure within 6 months (NYHA ¾ Grade), patients with untreated symptomatic arrhythmia or myocardial infarction history;

5. Individuals with malabsorption syndrome or other diseases affecting gastrointestinal absorption, and patients who need intravenous nutrition or cannot take orally or through nasogastric tube;

6. Participants who have received other SARS CoV-2 monoclonal antibody therapy or antiviral therapy (including research therapy);

7. Participants who received COVID-19 convalescent plasma therapy;

8. Patients receiving anti HIV treatment;

9. Participants who also participate in any other type of medical research or are considered to be scientifically or medically incompatible with this research;

10. Participants who have participated in the intervention clinical research in the past 30 days should pass 5 half lives or 30 days, whichever is longer, if the previous research intervention has a longer half life.

11. Researchers believe that the test will endanger any health and safety of participants;

12. Women who are pregnant, nursing or planning to be pregnant during the study period or men whose partners plan to be pregnant during the study period;

13. Unable to provide informed consent.Contacts and Locations.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Fuzhou General Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

zongyang yu, Ph.D

Role: PRINCIPAL_INVESTIGATOR

The 900th Hospital of the Joint Logistic Support Force, PLA

Locations

The 900th Hospital of the Joint Logistic Support Force, PLA

Fuzhou, Fujian, China

Site Status: RECRUITING

Countries

China

Central Contacts

Zongyang Yu, Ph.D

Role: CONTACT

yuzy527@sina.com

13509327806 ext. 22859650

Facility Contacts

zongyang yu, Ph.D

Role: primary

yuzy527@sina.com

13509327806 ext. 22859650

Other Identifiers

Innovation-A

Identifier Type: -

Identifier Source: org_study_id