Skip to content

A clinical study on the construction of a comfortable and painless bronchoscopic diagnosis and treatment anesthesia protocol based on ultrasound guidance

A clinical study on the construction of a comfortable and painless bronchoscopic diagnosis and treatment anesthesia protocol based on ultrasound guidance

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500102944
Enrollment
Unknown
Registered
2025-05-22
Start date
2025-05-25
Completion date
Unknown
Last updated
2025-05-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchoscopy is required for diagnosis and treatment of related diseases

Interventions

A group:General anesthesia is performed with drugs such as propofol, fentanyl, rocuronium, etc
B group:Ultrasound-guided nerve block and cricothyroid puncture combined with remimazolam
P group:Combination of propofol and esketamine
R group:Combination of remimazolam and esketamine
D group:Combination of dexmedetomidine and esketamine

Sponsors

First affiliated Hospital of Huzhou Normal College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Part One: 1. general bronchoscopy; Bronchoscopic biopsy, endotracheal endoscopic endoscopic tumor and lymph node biopsy; Endobronchial tumor interventional treatment for trachea, endobronchial stent implantation, balloon dilation; Patients with bronchoscopy for foreign bodies 2. Age 18~80 years old 3. ASA Classification I.-III 4. Body Mass Index (BMI) 18~30kg/m^2 Part Two: 1. Schedule bronchoscopy examination 2. ASA Classification I-II 3. Age 18-65 years old 4. Body Mass Index (BMI) 18-28 kg/m²

Exclusion criteria

Exclusion criteria: Part One: 1. Allergy to anesthetic drugs 2. Severe hypertension and arrhythmia, severe heart and lung dysfunction 3. Newly onset of myocardial infarction, unstable angina pectoris 4. Severe pulmonary hypertension 5. Severe coagulation disorder 6. Multiple bullae 7. Combined aortic aneurysm 8. Mental disorders 9. Refusal of the patient or family to participate Part Two: 1. Resting SpO2 < 93%, preoperative MAP < 60 mmHg, preoperative HR < 50 bpm 2. Severe cardiopulmonary dysfunction and severe hypertension, arrhythmia 3. Patients with severe liver and kidney dysfunction and/or coagulopathy 4. Patients with severe sleep apnea syndrome 5. Patients with potential or confirmed difficult airways 6. Patients with severe mental or cognitive, neurological dysfunction 7. Patients or family members refuse to participate 8. Patients allergic to the study drug.

Design outcomes

Primary

MeasureTime frame
Vital signs at each time point;Incidence of hypoxemia;

Secondary

MeasureTime frame
Onset of anesthesia;Wake time;Choking reaction;Incidence of hypoxemia;Patient and operating physician satisfaction;Minimum oxygen saturation;Vital signs at each time point;Total amount of esketamine;Number and amount of propofol supplements;Wake time;Incidence of perioperative adverse reactions;Patient and operating physician satisfaction;

Countries

China

Contacts

Public ContactWang Xinqiang

First affiliated Hospital of Huzhou Normal College

ddwxq218@163.com+86 139 6729 9603

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026