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Evaluation of the effect of taking tricholoma matsutake, cannabis sativa capsule and dendrobium candidum to nutrition intervention of patients with novel coronavirus pneumonia (COVID-19) during convalescence.

Evaluation of the effect of taking tricholoma matsutake, cannabis sativa capsule and dendrobium candidum to nutrition intervention of patients with novel coronavirus pneumonia (COVID-19) during convalescence.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030920
Enrollment
Unknown
Registered
2020-03-17
Start date
2020-02-20
Completion date
Unknown
Last updated
2020-03-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Novel Coronavirus Pneumonia (COVID-19)

Interventions

Tricholoma matsutake group:Taking tricholoma matsutake
Cannabis sativa capsule group:Taking cannabis sativa capsule
Dendrobium candidum group:Taking dendrobium candidum
Routine treatment group:Taking routine drugs and food

Sponsors

HwaMei Hospital, University of Chinese Academy of Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years old; 2. The person, who is diagnosed as COVID-19 according to the 'Diagnosis and treatment of novel coronavirus pneumonia (trial edition 5)', is treated with de-isolation and meets hospital discharge criteria: Temperature returned to normal over 3 days, respiratory symptoms improved obviously, two consecutive respiratory tract pathogenic nucleic acid detection negative (sampling time interval at least 1 day), can be removed from isolation and discharged or transferred to the corresponding department to treat other diseases; 3. The gastrointestinal structure and function of the patient are permitted and can be used safely and should be actively supported by enteral nutrition.

Exclusion criteria

Exclusion criteria: 1. Gestational female patients; 2. Patients with allergic constitution, specifically with a history of allergies to these three intervention drugs; 3. Patients with other malignant diseases such as malignant tumours, chronic liver or kidney diseases, and reaching the end stage; 4. Patients with known psychiatric disorders; 5. Patients withdrawing from other clinical trial within 4 weeks.

Design outcomes

Primary

MeasureTime frame
Albumin;Cellular immune indicators (total lymphocyte count (TLC) and T lymphocyte subsets (CD3, CD4));

Secondary

MeasureTime frame
Recurrence rate of COVID-19.;Height;Weight;body mass index;upper arm circumference;triceps fold thickness;transferrin concentration;prealbumin concentration;C-reactive protein;humoral immune indicators (serum IgA, IgG, IgM);inflammatory factors (including IL-2, IL-4, IL-6, IL-10, TNF-alpha, TNF-gama, etc.);

Countries

China

Contacts

Public ContactTing Cai

HwaMei Hospital, University of Chinese Academy of Sciences

caiting@ucas.ac.cn+86 13738498188

Outcome results

None listed

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