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临床试验/NCT07478484
NCT07478484招募中4 期

A Clinical Study on Sequential Infusion Versus Concomitant Infusion of Ceftazidime-avibactam Combined With Aztreonam for the Treatment of Metallo-β-lactamase-producing Carbapenem-resistant Gram-negative Bacterial Infections.

Jing Zhou1 个研究点 分布在 1 个国家目标入组 144 人开始时间: 2026年3月31日最近更新:
干预措施

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
144
试验地点
1
主要终点
Clinical cure rate

研究概览

简要总结

Metallo-β-lactamase-producing carbapenem-resistant Gram-negative bacteria (MBL-CR-GNB), due to their capacity to hydrolyze almost all β-lactam antibiotics, have become a critical global threat in antimicrobial resistance. Current novel β-lactamase inhibitors (e.g., avibactam, relebactam, vaborbactam) only inhibit serine enzymes and are ineffective against metallo-β-lactamases (MBL), severely limiting clinical treatment options. Aztreonam (ATM) is inherently stable against MBL, while avibactam (AVI) inhibits co-produced serine β-lactamases (e.g., KPC, OXA-48). Their combination achieves complementary synergistic antibacterial effects. The ceftazidime-avibactam plus aztreonam (CZA+ATM) regimen, operating via the mechanism of "avibactam protecting aztreonam", has demonstrated synergistic bactericidal activity against NDM, VIM, IMP and other MBL-producers in multiple real-world and clinical studies, significantly reducing infection-related mortality.However, although current domestic and international guidelines recommend the CZA+ATM combination for MBL infections, there is no consensus on optimal infusion strategies. Based on the above, this study hypothesizes that in patients with complicated infections caused by MBL-producing CR-GNB, different infusion modalities of ceftazidime-avibactam combined with aztreonam-concomitant infusion versus sequential infusion-will show no significant differences in PK/PD target attainment rates, clinical cure rates, microbiological eradication rates, or all-cause mortality, without increasing the risk of adverse events.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 100 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients diagnosed with complicated intra-abdominal infection (cIAI), hospital-acquired pneumonia (HAP), ventilator-associated pneumonia (VAP), complicated urinary tract infection (cUTI), or bloodstream infection (BSI);
  • Patients with confirmed infections caused by metallo-β-lactamase-producing carbapenem-resistant Gram-negative bacteria (MBL-CR-GNB), as determined by genotypic testing using next-generation sequencing (NGS) or carbapenem resistance gene testing;
  • Patients receiving treatment with ceftazidime-avibactam in combination with aztreonam.

排除标准

  • Patients aged under 18 years;
  • Patients with known hypersensitivity to ceftazidime, avibactam, aztreonam, or any of the excipients; or those with a history of severe hypersensitivity reactions (e.g., anaphylactic shock, severe skin reactions) to any other β-lactam antibacterial agents (such as penicillins, monobactams, or carbapenems);
  • Pregnant or breastfeeding women;
  • Patients unable to comprehend or comply with the study protocol;
  • Any other condition which, in the investigator's discretion, makes the patient unsuitable for participation in the trial.

研究组 & 干预措施

sequential infusion

Active Comparator

干预措施: ceftazidime-avibactam combined with aztreonam (Drug)

concomitant infusion

Experimental

干预措施: ceftazidime-avibactam combined with aztreonam (Drug)

结局指标

主要结局

Clinical cure rate

时间窗: 14 days

Clinical cure at Day 14 of treatment

次要结局

未报告次要终点

研究者

发起方
Jing Zhou
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jing Zhou

Chief Physician

The First Affiliated Hospital with Nanjing Medical University

研究点 (1)

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