Viewing Study NCT05813600



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Last Modification Date: 2024-10-26 @ 2:56 PM
Study NCT ID: NCT05813600
Status: COMPLETED
Last Update Posted: 2023-04-14
First Post: 2023-04-07

Brief Title: Efficacy and Safety of NirmatrelvirRitonavir for Treating Omicron Variant of COVID-19
Sponsor: Xiangao Jiang
Organization: Wenzhou Central Hospital

Study Overview

Official Title: To Evaluate the Efficacy and Safety of NirmatrelvirRitonavir in the Treatment of the Omicron Variant of COVID-19
Status: COMPLETED
Status Verified Date: 2023-04
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this clinical trial is to evaluate the efficacy and safety of NirmatrelvirRitonavir in the treatment of the Omicron variant of COVID-19 The main question it aims to answer is Whether the use of the drug can help patients recover from COVID-19

Patients in both groups were given Lianhua Qingwen Capsule orally 3 timesday 6 gtime oral antipyretic ibuprofen suspension 10ml and symptomatic supportive treatment for body temperature 385 The study group was given Nirmatrelvir 300mgRitonavir 100mg orally q12h for 5 days and the control group not given any antiviral drugs
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None