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A Comparative Study on the Application of Remimazolam in Awake Endotracheal Intubation in Patients

A Comparative Study on the Application of Remimazolam in Awake Endotracheal Intubation in Patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111193
Enrollment
Unknown
Registered
2025-10-27
Start date
2022-09-25
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

Difficult airway

Interventions

Remimazolam group (group R):Intravenous drip of remimazolam 0.15mg/kg
Dexmedetomidine group (group D):Patients in the dexmedetomidine group received an intravenous pump infusion of dexmedetomidine at a dose of 1.0 µg/kg
Midazolam group (group M):Patients in the midazolam group received an intravenous bolus of midazolam at a dose of 0.04 mg/kg

Sponsors

The First People’s Hospital of Jingzhou
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1.Age: 18-60 years old 2.BMI: 18.5-23.9kg/m ^2 3.ASA classification I-II. 4. Preoperative assessment of difficult airway (guideline criteria: Mallampati grade III or IV, mouth opening <3cm, nail and chin distance <6cm or less than the width of three transverse fingers of the examinee, the anterior extension of the lower jaw cannot align the upper and lower incisors, abnormal extension of the atlas joint, meeting any one of the above is acceptable)

Exclusion criteria

Exclusion criteria: 1.Allergic to benzodiazepines or flumacinib 2. People with airway hyperresponsiveness diseases (combined with chronic bronchitis, asthma and other respiratory diseases) 3. Fill your stomach 4. Reflux esophagitis, intestinal obstruction, etc 5. Have clinically relevant cardiovascular conditions (such as sinus bradycardia or severe arrhythmia) 6. People with neuropathy, mental illness or allergic diseases.

Design outcomes

Primary

MeasureTime frame
Intubation success rate;

Secondary

MeasureTime frame
Intubation Numbers;Eyelash reflex vanishing time;Time required for intubation;Record the patients' mean arterial pressure (MAP), heart rate (HR), and oxygen saturation (SpO2) at each time point: before induction (T0), before intubation (T1), immediately after intubation (T2), a;Postoperative complications;

Countries

China

Contacts

Public ContactTang Li

The First People’s Hospital of Jingzhou

462244408@qq.com+86 716 811 3627

Outcome results

None listed

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