Jinhua Qinggan Granules in the Treatment of COVID-19

About this trial

Last updated 4 years ago

Study ID

CRO-003-TCM- JHQG -2020/3.0

Status

Completed

Type

Interventional

Phase

Phase 2

Placebo

Accepting

18 to 75 Years

All Sexes

Trial Timing

Ended 5 years ago

What is this trial about?

The clinical trial is designed to be randomized, double blind, placebo controlled, to evaluate the effectiveness and safety of Jinhua Qinggan granules (JHQG) on mild-category patients of COVID-19 in Pakistani population with the age limit of 18-75 years, at10th day comprehensive follow-up. The informed consent form must be signed by the subjects before their participation in the trial.

What are the participation requirements?

Inclusion Criteria

* 1) Between the ages of 18-75 years, both 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 7.1.6).

* 4) The subject has signed the informed consent form;

Exclusion Criteria

* 1) Younger than 18 years or older than 75 years.

* 2) Patients with moderate or critical Coronavirus infection confirmed by real time RT-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.

* 3) 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;

* 4) With severe cardiopulmonary dysfunction, cardiopulmonary insufficiency.

* 5) Subjects, who took other antiviral, antibacterial, cough relieving, expectorant and antiasthmatic drugs within 3 days prior to the visit (including β2 receptor agonists, anticholinergic agents, theophylline drugs, glucocorticoids, expectorant and Chinese Medicine.)

* 6) Allergic individuals and those who are known to be allergic to experimental drugs

* 7) Pregnant women, lactating women or fertile women who are ready to conceive in 3 months.

* 8) Subject, who has participated in the past 1 month in another clinical study.

* 9) Subjects who are not suitable for the clinical trial based on investigators' judgment.