Tetrandrine Tablets Used in the Treatment of COVID-19

Corona Virus Disease 2019,COVID-19 Clinical Trial

— TT-NPC  

Official title:

Clinical Study of Tetrandrine Tablets Adjuvant Treatment With COVID-19

Clinical Trial Details — Status: Enrolling by invitation

Administrative data

• NCT number: NCT04308317
• Other study ID #: TT-NPC
• Status: Enrolling by invitation
• Phase: Phase 4
• Start date: March 5, 2020
• Est. completion date: May 1, 2021

Study information

• Verified date: March 2020
• Source: Henan Provincial People's Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The study is expected to treat patients with mild and severe neo-coronary pneumonia through standard treatment regimens in combination with tetrandrine tablets, thereby reducing the clinical progress of some patients, improving prognosis, reducing the incidence of pulmonary fibrosis during rehabilitation, and improving patients' quality of life.

Description:

Since December 2019, a number of cases of pneumonia infected with the new coronavirus have been found in wuhan, hubei province.Has now become a global epidemic of crisis.

After recent frontline anti-epidemic experience, the diagnostic and treatment specifications for new coronary pneumonia have been updated several times. In the latest country, "Specifications for the Diagnosis and Treatment of New Types of Coronary Pneumonia (Trial Version 6)", the traditional Chinese medicines have again emphasized For the treatment of patients, traditional Chinese medicine preparations such as Xuebijing and Qingfei Paidu Decoction have been recommended, but the introduction of anti-fibrosis related drugs is still lacking.Tetrandrine is a traditional Chinese medicine. Previous research has shown that it is an antagonist of calmodulin, has anti-tumor, anti-inflammatory effects, and can effectively inhibit fibroblasts, thereby inhibiting pulmonary fibrosis.The study is expected to treat patients with mild and severe neo-coronary pneumonia through standard treatment regimens in combination with tetrandrine tablets, thereby reducing the clinical progress of some patients, improving prognosis, reducing the incidence of pulmonary fibrosis during rehabilitation, and improving patients' quality of life.

Recruitment information / eligibility

• Status: Enrolling by invitation
• Enrollment: 60
• Est. completion date: May 1, 2021
• Est. primary completion date: March 1, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

Inclusion Criteria:

• Patients with mild and severe cases who have been diagnosed with new coronavirus pneumonia according to the "Pneumonitis Diagnosis and Treatment -

• Plan for New Coronavirus Infection"

• Age 18 to 75 years;

• Sign the informed consent voluntarily.

Exclusion Criteria:

• With active tuberculosis, idiopathic pulmonary fibrosis, bronchial asthma, bronchiectasis, pulmonary embolism, patients with chronic respiratory failure or other severe respiratory disease;

• According to the "pneumonia diagnosis and treatment program for new coronavirus infection" (trial version 6), critically ill patients

• With severe patients with disease of heart head blood-vessel, malignant arrhythmia, unstable angina, acute myocardial infarction and death, cardiac function level 3 and above, stroke, cerebral hemorrhage, etc.);

• With severe liver and kidney diseases (severe liver disease refers to cirrhosis, portal hypertension and varices bleeding, severe kidney disease including dialysis, kidney transplantation);

• Pregnant and lactating women;

• Severe cognitive and mental disorders;

• Clinical investigators who were participating in other interventions within 1 month prior to inclusion

Related Conditions & MeSH terms

• Corona Virus Disease 2019,COVID-19
• Virus Diseases

Intervention

Drug:
• Tetrandrine
Tetrandrine 60mg QD for 1week

Locations

Country	Name	City	State
China	Tetrandrine Tablets	Jinhua	Zhejiang

Sponsors (1)

Lead Sponsor	Collaborator
Henan Provincial People's Hospital

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Survival rate	Death event	12 weeks
Secondary	body temperature	inflammatory indicator	2 weeks