Polycolistin E Sodium Mesylate Combined With Intravenous Atomization for Carbapenem Resistant Gram-negative Bacteria in Pulmonary Infection

NCT ID: NCT06907069

Last Updated: 2025-04-02

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ENROLLING_BY_INVITATION

Clinical Phase

PHASE4

Total Enrollment

200 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-01-01

Study Completion Date

2025-12-31

Brief Summary

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Pulmonary infection is a kind of infectious disease that seriously damages human health. It usually starts quickly and progresses rapidly in clinical manifestations, and is often accompanied by upper respiratory tract infection symptoms. With the increasing use of broad-spectrum antibiotics in clinical practice, the failure of anti-infection caused by drug-resistant bacteria is more and more common. Once a patient develops carbapenem-resistant gram-negative bacteria (CRO) infection, there are limited drug options. Therefore, HAP, as a serious and common complication, has a high incidence and mortality for ICU patients. In this study, patients who met the diagnostic criteria for pulmonary infection caused by CRO that was clearly or strongly suspected to be resistant to carbapenems but sensitive to CMS were selected, and the combined treatment regimen of CMS intravenous atomization was adopted. To explore the therapeutic effect of CMS combined with intravenous atomization in patients with carbapenem resistant gram-negative bacteria in lung infection. To evaluate the safety and tolerability of the combination regimen in patients with pulmonary infections caused by CRO. The purpose of this study was to explore the efficacy and safety of CMS combined with intravenous atomization in the treatment of patients with CRO induced pulmonary infection, and to provide a basis for its clinical rational application.

Detailed Description

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Conditions

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Lung Infection Bacterial

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Intravenously atomized polycolistin E sodium mesylate

Group Type EXPERIMENTAL

Intravenously atomized polycolistin E sodium mesylate

Intervention Type DRUG

To explore the therapeutic effect of CMS combined with intravenous atomization in patients with carbapenem resistant gram-negative bacteria in lung infection.

Interventions

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Intravenously atomized polycolistin E sodium mesylate

To explore the therapeutic effect of CMS combined with intravenous atomization in patients with carbapenem resistant gram-negative bacteria in lung infection.

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

1. Voluntarily participate in the study and sign the informed consent;
2. Inpatients aged 18-80 years old, regardless of gender;
3. Patients who met the diagnostic criteria for pulmonary infection in the Guidelines for the Diagnosis and Treatment of Hospital-Acquired Pneumonia and Ventilator-Associated Pneumonia for Adults in China (2018 Edition);
4. Infections caused by Gram-negative bacteria (CRO) that are known or strongly suspected to be resistant to carbapenems but sensitive to CMS.

Exclusion Criteria

1. Age \> 80 years old;
2. The patient had a history of severe allergy or hypersensitivity to polymyxins;
3. Patients with serious dysfunction of heart, liver, kidney and other important organs;
4. Patients with serious diseases such as malignant tumors and blood system diseases;
5. Patients with low immune function and risk of opportunistic pathogen infection;
6. Patients who used excessive colistin intravenous or atomized inhalation therapy within 72h before enrollment;
7. Have participated in other clinical trials within three months;
8. Pregnant or breastfeeding women;
9. There are other circumstances that the researcher believes are not suitable for inclusion.
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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First Affiliated Hospital of Ningbo University

NETWORK

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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The First Affiliated Hospital of Ningbo University

Ningbo, Z, China

Site Status

Countries

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China

Other Identifiers

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2024-R044-02

Identifier Type: -

Identifier Source: org_study_id

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