Skip to content

Open label randomized controlled small sample study of lentinan nasal drops in the treatment of upper respiratory tract infection of COVID-19 Omicron mutant

Open label randomized controlled small sample study of lentinan nasal drops in the treatment of upper respiratory tract infection of COVID-19 Omicron mutant

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070776
Enrollment
Unknown
Registered
2023-04-23
Start date
2022-06-10
Completion date
Unknown
Last updated
2023-06-04

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

no-treatment control group:Shufeng Jiedu Capsules (COVID-19 recommended general treatment plan for the ninth version)
Treatment group 1:Lentinan 25ug/d×5 days+Shufeng Jiedu Capsules (COVID-19 recommended general treatment plan for the ninth version)
Treatment group 2:Lentinan 50ug/d×5 days+Shufeng Jiedu Capsules (COVID-19 recommended general treatment plan for the ninth version)
Treatment group 3:Lentinan 100ug/d×5 days+Shufeng Jiedu Capsules (COVID-19 recommended general treatment plan for the ninth version)

Sponsors

The First Affiliated Hospital of Naval Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Voluntary signing of informed consent form 2. At least 18 years old but less than 60 years old; Gender unlimited 3. Within 5 days prior to screening, with or without COVID-19 related symptoms, SARS-CoV-2 infection was confirmed through PCR detection within 24 hours; 4. Agree not to participate in other interventional clinical trials for the treatment of SARS-CoV-2 during the study period 5. Agree to the detailed sampling requirements in the evaluation schedule and comply with the research requirements

Exclusion criteria

Exclusion criteria: 1. COVID-19 positive patients; 2. Patients with bleeding tendencies 3. Allergy to shiitake mushroom polysaccharides or their pharmaceutical components; 4. Have experienced severe allergic reactions, including systemic urticaria, vascular edema, and hypersensitivity reactions 5. Received COVID-19 rehabilitation plasma and SARS-CoV-2 antibody treatment; 6. Have received other investigational drugs for the treatment of COVID-19; 7. Pregnant or lactating women; 8. Those who merge with other serious systemic diseases; 9. According to the judgment of the researcher, it is deemed unsuitable to participate in this study;

Design outcomes

Primary

MeasureTime frame
Virus negative rate;

Secondary

MeasureTime frame
Difference in viral load in nasopharyngeal swabs/respiratory secretions after medication;Hospital discharge rate;Clinical outcome;

Countries

China

Contacts

Public ContactXuesong Liang

Department of Infectious Diseases, Changhai Hospital Affiliated to Naval Military Medical

liangxuesong2000@163.com+86 13764998573

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026