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Study on clinical application of Remazolam in outpatient painless gastroenteroscopy

Effect of Remazolam combined with butorfenol tartrate in outpatient painless gastroenteroscopy

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000038876
Enrollment
Unknown
Registered
2020-10-08
Start date
2020-10-12
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Painless digestive endoscopy

Interventions

Group A :Butorphanol tartrate 0.6mg combined with propofol 1.5-2mg/kg
Group B :Butorphanol tartrate 0.6mg combined with remazolam 0.2mg/kg
Group C :Butorphanol tartrate 0.6mg combined with remazolam 0.3mg/kg

Sponsors

Yancheng First People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. The age of 30-65 is not limited to men and women; 2. Patients with BMI of 18-30kg / m2; 3. Patients with ASA grade I or II; 4. Patients whose estimated operation time is less than 30 minutes; 5. All patients signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients allergic to benzodiazepines; 2. Preoperative evaluation of patients with difficult airway (Mallampati grade >= grade III) or sleep apnea syndrome; 3. Patients with previous history of angina pectoris and arrhythmia; 4. Patients with long-term use of sedative hypnotics; 5. Other circumstances in which the researcher judged that the patient was not suitable to participate in the clinical trial.

Design outcomes

Primary

MeasureTime frame
Anesthesia effect;

Secondary

MeasureTime frame
Blood pressure;Pulse oxygen saturation;Heart rate;BIS;The injection pain;Nausea and vomiting;drowsiness;Full wake time;Narcotic dosage;Dosing frequency;

Countries

China

Contacts

Public ContactYingying Zhao

Yancheng Clinical College affiliated to Xuzhou Medical University

1067840706@qq.com+86 18752110638

Outcome results

None listed

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