Clinical trial

An Observational Study on the Efficacy and Safety of the Combination Regimen Based on Eravacycline in the Treatment of Multidrug-resistant Bacterial Infections in Immunocompromised Host Populations.

Name
LPan20230578
Description
The goal of this observational study is to explore the treatment mode and clinical outcome of patients with immunocompromised who received the combined regimen of eraracycline in the treatment of multidrug-resistant bacterial infections, to evaluate the efficacy and safety of the combined regimen of eravacycline in the treatment of multidrug-resistant bacterial infections in immunocompromised host populations, and to provide data reference for the treatment of immunocompromised populations.
Trial arms
Trial start
2024-02-01
Estimated PCD
2025-12-31
Trial end
2025-12-31
Status
Not yet recruiting
Treatment
Eravacycline
There is no other intervention.
Other names:
XERAVA
Size
100
Primary endpoint
30-day all-cause mortality
during the treatment (1-14 days); the end of treatment(Day 14); 28-35 days after first dose
Clinical cure rate
during the treatment (1-14 days); the end of treatment(Day 14); 28-35 days after first dose
Symptom improvement rate
during the treatment (1-14 days); the end of treatment(Day 14); 28-35 days after first dose
Eligibility criteria
Inclusion Criteria: * ≥ 18 years old. * Voluntary to participate in this study and signed informed consent. If the subject is unable to read and / or sign the informed consent due to incapacity or other reasons, the guardian of the subject is required to act as the agent of the informed process and sign the informed consent. * In a state of low immune function: * In this study, if the patient meets any of the following criteria, the patient 's immune function is considered to be low : 1 patients who have previously received solid organ transplantation ( liver, kidney, lung, heart ) ; 2 hematological malignancies ( leukemia, lymphoma ) ; 3 Patients received long-term immunosuppressive therapy, or used steroids that reached immunosuppressive doses within 21 months before screening ( ≥ 10 mg prednisone or \> 15 mg / kg / d hydrocortisone or d \> 3 mg / kg / d methylprednisolone, continuous d \> 5 days ) \[ 4,13 \]. 4 Severe infections occurred recently, leading to extremely low immune function. * Infections caused by known or highly suspected multidrug-resistant pathogens (MDR), or gram-negative bacteria that are sensitive to eravacycline in adult patients with limited treatment options. The high-risk factors and standards of MDR met the definition of " Chinese expert consensus on prevention and control of nosocomial infection of multidrug-resistant bacteria "; multidrug-resistant bacteria (MDR) refer to bacteria that are resistant to three or more types of commonly used antibiotics that are usually sensitive. Multidrug resistance also includes pan-drug resistance (XDR) and pan-drug resistance (PDR). * Patients treated with elastin ≥ 3 days. Exclusion Criteria: * Urinary tract infection. * Clear culture results showed that microbial pathogens were not sensitive to test drugs (such as Pseudomonas aeruginosa, etc.). * Patients whose expected survival time cannot exceed the study period. * The researchers believe that there is any medical history, current condition, treatment, abnormal laboratory examination or other conditions that may affect the test results, interrupt the test process (or the subject cannot complete all the operations and visits required by the test) or accept the test drugs that will increase the risk of the subject. Patients with end-stage diseases have immediate life-threatening disease evidence. * Patients with a history of allergic reactions to tetracyclines or any adjuvant contained in the study drug formula. * Vulnerable groups other than critically ill patients, including people with mental illness, cognitive impairment, pregnant women, etc.
Protocol
{'studyType': 'OBSERVATIONAL', 'patientRegistry': False, 'designInfo': {'observationalModel': 'COHORT', 'timePerspective': 'PROSPECTIVE'}, 'bioSpec': {'retention': 'SAMPLES_WITHOUT_DNA', 'description': 'Abdominal drainage fluid samples, blood samples, respiratory tract samples'}, 'enrollmentInfo': {'count': 100, 'type': 'ESTIMATED'}}
Updated at
2024-01-25

1 organization

1 product

1 indication