Real-World antibiotic study cut short: what we can learn
NCT ID NCT05487586
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study tracked how the antibiotic ceftazidime-avibactam is used in real hospital settings in China for serious infections like pneumonia and abdominal infections. Researchers planned to enroll 450 patients but the study was terminated early. The goal was to see how often the drug clears the infection and how bacteria respond, providing insights for doctors.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- ceftazidime-avibactam
- What this could lead to
- If successful, this study could provide real-world data on how well ceftazidime-avibactam works against tough hospital infections in everyday practice.
- What could go wrong
- This was an observational study that was terminated early, so results may be limited. It does not test a new treatment, only observes current use.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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220 people
The number who actually took part.
- Started
-
Oct 2022
- Finished
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Jul 2024
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Hospitalized patients treated with CAZ AVI for ≥1 dose in approximately 20 study sites.
- Ages
-
18 years and older
- Sex
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Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion criteria: * Initiate ≥1 dose of ceftazidime-avibactam during hospitalization. * Aged ≥ 18 years old at the time of the informed consent signature. * Provide signed informed consent. Exclusion criteria: * Are enrolled in any clinical trial, including enrollment in non interventional studies. * Pregnant women.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Beijing Tsinghua Changgung Hospital
Beijing, China
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Henan Provincial People's Hospital
Zhengzhou, China
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Huashan Hospital Fudan University
Shanghai, Shanghai Municipality, 200040, China
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Shanghai Tenth People's Hospital
Shanghai, China
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Sir Run Run Shaw Hospital, Zhejiang University School of Medicine
Hangzhou, China
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The Affiliated People's Hospital of Ningbo University
Ningbo, China
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The First Affiliated Hospital of Nanchang University
Nanchang, China
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The First Affiliated Hospital of Soochow University
Suzhou, China
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The First Affiliated Hospital of Xi'an Jiaotong University
Xi'an, China
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The First Affiliated Hospital, Sun Yat-sen University
Guangzhou, China
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The First affiliated Hospital of Anhui Medical University
Hefei, China
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The Second Affiliated Hospital of Zhejiang University School of Medicine
Hangzhou, China
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The Second People's Hospital of Hebei Medical University
Shijiazhuang, China
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The Third Hospital of Hebei Medical University
Shijiazhuang, China
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Tianjin Medical University General Hospital
Tianjing, China
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Xiangya Hospital Central South University
Changsha, China
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Zhongda Hospital Southeast University
Nanjing, China
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