Clinical Trials Directory

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UnknownNCT05625022

Lianhua Qingke for the Rehabilitation of Patient With Omicron Infection

Efficacy and Safety of Lianhua Qingke in the Long-term Rehabilitation of Patients With Omicron Infection: a 6-month Follow-up Study

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
2,000 (estimated)
Sponsor
Qilu Hospital of Shandong University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The patients with Omicron infection usually have fever, respiratory symptoms, tachycardia, headache, toothache, muscle soreness, physical decline, and so on, while others are asymptomatic patients. It is urgent to find drugs to improve the long-term rehabilitation of symptomatic patients with Omicron infection and decrease the duration of viral shedding in both symptomatic and asymptomatic patients. This study aims to investigate the efficacy and safety of Lianhua Qingke tablets in patients with Omicron infection. The duration of viral shedding and symptoms will be evaluated. 6-month follow-up will be performed to evaluate the effect of Lianhua Qingke on long-term rehabilitation of all symptoms induced by Omicron infection, as well as infection events.

Conditions

Interventions

TypeNameDescription
DRUGLianhua Qingke tabletsLianhua Qingke tablets: 4 tablets once, three times daily

Timeline

Start date
2022-11-01
Primary completion
2023-06-30
Completion
2023-12-31
First posted
2022-11-22
Last updated
2022-11-22

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT05625022. Inclusion in this directory is not an endorsement.