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Traditional Chinese Medicine in the treatment of novel coronavirus pneumonia (COVID-19): a multicentre, randomized controlled trial

Traditional Chinese Medicine in the treatment of novel coronavirus pneumonia (COVID-19): a multicentre, randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030034
Enrollment
Unknown
Registered
2020-02-21
Start date
2020-02-07
Completion date
Unknown
Last updated
2020-02-25

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

Experimental group:TCM+Routine treatment of Western Medicine

Sponsors

Tongde Hospital of Zhejiang Province
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: (1) Patients in accordance with the diagnostic criteria of "Quick reference guide for diagnosis and treatment of novel coronavirus pneumonia(2019-nCoV)(Standard Edition)" and "Diagnostic and treatment protocols of novel coronavirus pneumonia(Trial version 5)" issued by National Health Commission; (2) Patients in accordance with the TCM syndrome differentiation standard; (3) Aged 18 to 85 years; (4) Before the trial begins, patients or their legal representatives voluntarily agree to participate by giving written informed consent approved by ethic committee.

Exclusion criteria

Exclusion criteria: (1) Diagnosed with other known viral pneumonia,like influenza virus, parainfluenza virus, adenovirus, respiratory syncytical virus, rhinovirus, human metapneumovirus and SARS coronavirus, etc.; (2) Diagnosed with mycoplasma pneumonia, chlamydial pneumonia and bacterial pneumonia; (3) Diagnosed with vasculitis, dermatomyositis, organizing pneumonia and other noninfectious diseases; (4) pregnant or breastfeeding woman; (5) Known to be allergic to this medicine ingredient; (6) Patients with serious underlying disease, and researchers considered inappropriate to participate.

Design outcomes

Primary

MeasureTime frame
Body temperature;TCM syndrome integral;Murray lung injury score;The transition time of novel coronavirus nucleic acid;MuLBSTA score;

Countries

China

Contacts

Public ContactKequn Chai

Tongde Hospital of Zhejiang Province

ckqmzygzs@163.com+86 13906503739

Outcome results

None listed

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