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Effects of Remimazolam versus Propofol on Emergence Agitation in Adult Patients Undergoing Otolaryngologic Surgery

Effects of Remimazolam versus Propofol on Emergence Agitation in Adult Patients Undergoing Otolaryngologic Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600116130
Enrollment
Unknown
Registered
2026-01-06
Start date
2026-01-06
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Emergence Agitation

Interventions

Remazolam group:Anesthetic maintenance with remimazolam
Propofol group:Anesthetic maintenance with propofol

Sponsors

Shanghai Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Age: 18-65 years old; 2.ASA I-II grade; 3.BMI: 18-30kg/m^2 4. The estimated duration of the operation is about 1 hour. 5. Preoperative airway assessment is acceptable, and it is expected that there is no risk of difficult ventilation or difficult intubation. 6. Good basic oxygenation: At rest, the pulse oxygen saturation when breathing air is >=96%. 7. Informed consent of the subjects.

Exclusion criteria

Exclusion criteria: 1. Have a history of mental illness or frequently take psychotropic drugs; 2. There were severe organic lesions in the heart or brain before the operation; 3. Allergy to propofol or benzodiazepines; 4. Inability to communicate due to hearing or language impairments; 5. Preoperative heart rate less than 50 beats per minute or second-degree or above atrioventricular block; 6. Possessing diseases that are prone to causing respiratory depression, such as chronic obstructive pulmonary disease, asthma, and sleep apnea syndrome.

Design outcomes

Primary

MeasureTime frame
Emergence Agitation;

Secondary

MeasureTime frame
Number of patients with different agitation scores and the highest agitation score recorded;Pain score;Time to emergence;Extubation time;Anxiety score;Sleep quality score;Nausea and vomiting;Adverse events;Quality of Recovery score (QoR score);Anesthesia satisfaction;

Countries

China

Contacts

Public ContactJianhui Liu

Shanghai Tongji Hospital

jianhuiliu_1246@163.com+86 136 6145 2939

Outcome results

None listed

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