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NCT05625022

Lianhua Qingke for the Rehabilitation of Patient With Omicron Infection

Status unknown Phase 4 Last updated 22 November 2022
What this trial tests

Phase 4 trial testing Lianhua Qingke tablets in Coronavirus in 2,000 participants. Status unknown.

Timeline
1 November 2022
Primary endpoint
30 June 2023
31 December 2023

Quick facts

Lead sponsorQilu Hospital of Shandong University
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment2,000
Start date1 November 2022
Primary completion30 June 2023
Estimated completion31 December 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Qilu Hospital of Shandong University

Who can join

18 and older, any sex, with Coronavirus or Traditional Chinese Medicine. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Coronavirus

Currently open trials in the same condition.

Other Qilu Hospital of Shandong University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05625022.

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