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Study identifier: NCT07395596 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Remimazolam for Bronchoscopy in High-Risk Patients

Condition: Pulmonary Infection · Pulmonary Nodule · Phthisis  ·  Sponsor: First Affiliated Hospital of Zhejiang University

PhasePhase 4
Planned participants360
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Bronchoscopy is currently widely used for the diagnosis and treatment of various respiratory diseases. However, the operation of bronchoscopy is irritating, causes a strong stress response, and shares the airway with the patient, making the patient highly susceptible to respiratory and cardiovascular risks. Among these risks, hypoxia is the most common adverse event.Different drug regimens can be selected for anesthesia under deep sedation. The combination of analgesic agents can help reduce coughing during bronchoscopy. Therefore, we employ a combination of sedative and analgesic drugs for painless bronchoscopy procedures. Among sedatives, propofol is the most commonly used. However, due to its disadvantages, such as respiratory and circulatory depression, we have introduced a novel approach combining remimazolam for sedation. The aim is to investigate whether this new regimen, compared to traditional propofol-based sedation, can reduce the incidence of hypoxia, minimize circulatory depression, and lead to faster postoperative awakening and recovery. Additionally, we hope to observe fewer adverse events, such as perioperative nausea and vomiting, excessive secretions, dizziness, and chills.

This description comes directly from the study's public registry record.

Talk to the study team

Yueying Zheng  ·  +8613777408863  ·  1507128@zju.edu.cn

Yeke Zhu  ·  +8613515815457  ·  21618018@zju.edu.cn

Always discuss trial participation with your own doctor first.

Locations (2)

The First Affliated Hospital, Zhejiang University School Of MedicineHangzhou, Zhejiang, ChinaRecruiting
Shaoxing City First People's HospitalShaoxing, Zhejiang, ChinaNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07395596