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Evaluation of the efficacy and safety of remazolam besylate combined with esketamine in bronchoscopy

Evaluation of the efficacy and safety of remazolam besylate combined with esketamine in bronchoscopy

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063338
Enrollment
Unknown
Registered
2022-09-05
Start date
2022-12-30
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

Anesthesiology

Interventions

Group DE:Dexmedetomidine combined with esketamine

Sponsors

Inner Mongolia Erdos Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age 45 to 65 years; American Society of anesthesiologists (ASA) class I-II; SpO2 > 90%

Exclusion criteria

Exclusion criteria: Known local anesthetic allergy history (remazolam besylate, esmketamine, dexmedetomidine, midazolam, propofol); Previous pulmonary diseases (such as chronic obstructive pulmonary disease (COPD), respiratory failure and asthma); Severe sleep apnea syndrome (apnea hypopnea index > 40); Chronic renal failure (glomerular filtration rate 30 kg/m^2); Allergic to the drugs used in the study

Design outcomes

Primary

MeasureTime frame
Operation completion success rate;

Secondary

MeasureTime frame
General information of the patient;Hemodynamics;Intraoperative anesthetic and vasoactive drug dosage;Time indicator;Infusion volume, intubation conditions, number of people needing remedial drugs;Mean oxygen saturation, minimum oxygen saturation, cough severity;Patient and bronchoscope physician satisfaction score;

Countries

China

Contacts

Public ContactWei Li

Erdos CentrHospital of Inner Mongolia Autonomous Region

732719139@qq.com+86 15204778880

Outcome results

None listed

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