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Multi-center, Randomized, Double Blind and Placebo Controlled Clinical Trial on the Efficacy and Safety of Jinhua Qinggan Granules (JHQG) for the Treatment of COVID-19 Patients.

Multi-center, Randomized, Double Blind and Placebo Controlled Clinical Trial on the Efficacy and Safety of Jinhua Qinggan Granules (JHQG) for the Treatment of COVID-19 Patients.

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000003697
Enrollment
Unknown
Registered
2020-08-25
Start date
2020-09-01
Completion date
Unknown
Last updated
2023-02-20

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

Sponsors

Center for Bioequivalence Studies and Clinical Research,Beijing Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-75 years male and female; 2. Confirmed Coronavirus infection by real time RT-PCR; 3. Mild cases of Coronavirus having main symptoms with minimum 2 grade (as mentioned in 7.1.2); 4. The subject has signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with moderate or critical Coronavirus infection confirmed by real time RT-PCR (rRT-PCR); cases meeting any of the following criteria: (1) Lung lesions; (2) Respiratory failure and requiring mechanical ventilation; (3) Shock; (4) With other organ failure that requires ICU cares; 2. Severe primary health conditions associated with cardiovascular, cerebrovascular, pulmonary, hepatic, renal, endocrine and hematological diseases, hematopoietic system (above grade II of cardiac function; ALT & AST are 1.5 times higher than the normal value; Creatinine above the upper limit of normal value) and mental illness or serious diseases affecting their survival, such as cancer or AIDS; 3. With severe cardiopulmonary dysfunction, cardiopulmonary insufficiency; 4. Subjects, who took other antiviral, antibacterial, cough relieving, expectorant and antiasthmatic drugs within 3 days prior to the visit (including ß2 receptor agonists, anticholinergic agents, theophylline drugs, glucocorticoids, expectorant and Chinese Medicine.); 5. Allergic individuals and those who are known to be allergic to experimental drugs; 6. Pregnant women, lactating women or fertile women who are ready to conceive in 3 months; 7. Subject, who has participated in the past 1 month in another clinical study; 8. Subjects who are not suitable for the clinical trial based on investigators judgment.

Design outcomes

Primary

MeasureTime frame
Change (improvement) in clinical signs and symptoms;Negative test time for SARS-CoV2 on RT-PCR;

Secondary

MeasureTime frame
Observation of body temperature: The onset time of fever and the complete time of defervescence.;Quality of Life Criterion;Chang in white blood cells, C-reactive protein and ferritin.;Change in radiographic findings of the lungs.;

Countries

Pakistan

Contacts

Public ContactProf. Dr M. Raza Shah T.I./Liu Qing Quan
raza.shah@iccs.edu+92 21 99261717 (Ext. 233, 530)

Outcome results

None listed

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