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Staphylococcus and Neisseria Tablets in the Treatment of Acute Exacerbations of Chronic Obstructive Pulmonary Disease. - Trial NCT05543343

Access comprehensive clinical trial information for NCT05543343 through Pure Global AI's free database. This phase not specified trial is sponsored by Qu Yiqing and is currently Recruiting. The study focuses on Pulmonary Disease, Chronic Obstructive. Target enrollment is 495 participants.

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NCT05543343
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Trial Details
ClinicalTrials.gov โ€ข NCT05543343
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Staphylococcus and Neisseria Tablets in the Treatment of Acute Exacerbations of Chronic Obstructive Pulmonary Disease.
Evaluating the Efficacy and Safety of Staphylococcus and Neisseria Tablets in the Treatment of Acute Exacerbations of Chronic Obstructive Pulmonary Disease.

Study Focus

High dose or normal dose staphylococcus albicans

Interventional

drug

Sponsor & Location

Qu Yiqing

Qilu Hospital of Shandong University

Jinan, China

Timeline & Enrollment

N/A

Jan 05, 2022

Aug 01, 2023

495 participants

Primary Outcome

Number of acute exacerbations of chronic obstructive pulmonary disease in 1 year

Summary

It is planned to enroll 495 acute exacerbation of chronic obstructive pulmonary disease
 patients, and they will be randomly assigned to the high-dose test group, normal dose test
 group or control group at a ratio of 1:1:1, with 165 patients in each group. The course of
 treatment is 90 days, and the total follow-up time is one year. The purpose of the study is
 to evaluate the effectiveness and safety of different doses of bacterial lysates
 (Staphylococcus and Neisseria Tablets) in the treatment of acute exacerbation of chronic
 obstructive pulmonary disease.

ICD-10 Classifications

Chronic obstructive pulmonary disease, unspecified
Other chronic obstructive pulmonary disease
Other specified chronic obstructive pulmonary disease
Chronic obstructive pulmonary disease with acute exacerbation, unspecified
Chronic obstructive pulmonary disease with acute lower respiratory infection

Data Source

ClinicalTrials.gov

NCT05543343

Non-Device Trial