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Traditional Chinese Medicine for Severe COVID-19

A Retrospective Cohort Study to Evaluate the Efficacy and Safety of Traditional Chinese Medicine as an Adjuvant Treatment for Patients With Severe COVID-19

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04323332
Enrollment
50
Registered
2020-03-26
Start date
2020-03-31
Completion date
2020-04-30
Last updated
2020-03-26

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

Conditions

COVID-19

Keywords

COVID-19, Traditional Chinese Medicine, Pneumonia, Coronavirus

Brief summary

In December 2019, a new type of pneumonia, COVID-2019 outbroke in Wuhan ,China, and currently the infected has been reported in more than at least 75 countries. Patients with severe COVID-19 have rapid disease progression and high mortality rate. This may attribute to the excessive immune response caused by cytokine storm. Strategies based on anti-virus drugs and treatments against symptoms have now been employed. However, these managements can't effectively treat the lethal lung injury and uncontrolled immune responses, especially in the elderly with severe COVID-19. Traditional Chinese Medicine (TCM), which treats the disease from anther perspective, has achieved satisfactory results. National Health Commission of China released a series of policies to enhance the administration of TCM prescriptions. This study is aimed to evaluate the efficacy and safety of Traditional Chinese Medicine as an adjuvant treatment for severe COVID-19.

Interventions

Traditional Chinese Medicine Prescriptions have been recommended according to the Guidelines for the treatment of COVID-19 issued by National Health Commission of the PRC.

Sponsors

Xiyuan Hospital of China Academy of Chinese Medical Sciences
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 85 Years
Healthy volunteers
No

Inclusion criteria

Key Inclusion Criteria: 1. Patients were diagnosed as severe COVID-19 according to the Coronavirus disease (COVID-19) Treatment Guidance (Six edition) 2. Patients received a combined treatment of TCM and conventional therapy, or only conventional therapy. Key

Exclusion criteria

1. Age \>85 years 2. After cardiopulmonary resuscitation 3. Patients combined with other organ failure or conditions need ICU monitoring and treatment, such as severe liver disease, severe renal dysfunction, upper gastrointestinal hemorrhage, disseminated intravascular coagulation. 4. Respiratory failure and need mechanical ventilation

Design outcomes

Primary

MeasureTime frame
Length of hospital stay (days)First treatment date up to 3 months

Secondary

MeasureTime frameDescription
CT imaging changesFirst treatment date up to 3 months
Mortality rateFirst treatment date up to 3 months
Time to Clinical Improvement (TTCI)First treatment date up to 3 months
The pneumonia severity index scoresFirst treatment date up to 3 monthsThe pneumonia severity index is a clinical tool helping in the risk stratification of patients with community-acquired pneumonia. It ranges from 0-395 scores and a higher score indicates higher death risk.
Time to COVID-19 nucleic acid testing negativity in throat swabFirst treatment date up to 3 months
Blood immune cell countBaseline, 7 and/ or 14 daysChanges in leukocyte, neutral, lymphocyte counts and absolute lymphocyte count from baseline
Serum inflammatory markersBaseline, 7 and/ or 14 daysChanges in blood interleukin-6, c-reactive protein,SS-A/Ro antibodies and serum ferritin from baseline.
Duration (days) of supplemental oxygenationFirst treatment date up to 3 months
Platelet and D-dimer changesBaseline, 7 and/ or 14 daysChanges in platelets and D-dimers from baseline.
Creatinine changesBaseline, 7 and/ or 14 daysChanges in serum creatinine from baseline.
Muscle enzymes changesBaseline, 7 and/ or 14 daysChanges in serum muscle enzymes from baseline, including alanine aminotransferase , AST, creatine kinase, LDH.
Usage of antibioticsFirst treatment date up to 3 monthsDosing time and amounts of antibiotics;the categories of the antibiotics
Usage of glucocorticoidsFirst treatment date up to 3 monthsDosing time and amounts of glucocorticoids
Frequency of adverse eventsFirst treatment date up to 3 months
Erythrocyte sedimentation rateBaseline, 7 and/ or 14 daysChanges in erythrocyte sedimentation rate from baseline.

Countries

China

Contacts

Primary ContactHao Li, Professor
xyhplihao1965@126.com+0086-133113382093

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026