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Study for integrated traditional Chinese and western medicine in the treatment of the fever period of epidemic hemorrhagic fever

Study for integrated traditional Chinese and western medicine in the treatment of the fever period of epidemic hemorrhagic fever

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027657
Enrollment
Unknown
Registered
2019-11-23
Start date
2019-12-01
Completion date
Unknown
Last updated
2019-11-25

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

Conditions

Epidemic hemorrhagic fever(Hemorrhagic fever with renal syndrome)

Interventions

Experimental group 1:Western medicine basic treatment combined with “Qingyi No. 1 granule”
Experimental group 2:Western medicine basic treatment combined with “Qingyi No. 2 granule”

Sponsors

Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: (1) Comply with the diagnostic criteria for epidemic hemorrhagic fever. (2) Patients with epidemic hemorrhagic fever in the fifth stage of fever period, body temperature = 38 ° C, and the time of fever should be <=72 h; (3) Comply with the diagnostic criteria of TCM syndrome (both Wei and Qi Phases); (4) Aged 18 to 70 years old; (5) History of allergic reactions without related drugs. (6) Under the premise of fully understanding the study, voluntarily accept the treatment and detection of the treatment plan of this study, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with abnormal liver function (AST, ALT exceeds the upper limit of normal by 5 times or more); (2) Patients with chronic kidney disease; (3) Combined with serious primary diseases such as cardiovascular and hematopoietic diseases, hematopoietic system, digestive ulcer disease, or serious diseases (such as tumors) that affect their survival; (4) Those who are allergic to drugs in the Chinese herbal compound; (5) Pregnant or lactating women; (6) Mentally or legally disabled patients.

Design outcomes

Primary

MeasureTime frame
Early intervention to reduce the incidence of critical illness (shock/kidney failure);

Secondary

MeasureTime frame
Antipyretic onset time and complete antipyretic time;

Countries

China

Contacts

Public ContactZheng Peiyong

Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine

zpychina@sina.com+86 18917763468

Outcome results

None listed

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