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Analysis of Risk Factors and New Prevention and Treatment Strategies for Adverse Events Related to Anesthesia Outside the Operating Room

Analysis of Risk Factors and New Prevention and Treatment Strategies for Adverse Events Related to Anesthesia Outside the Operating Room

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128551
Enrollment
Unknown
Registered
2026-07-22
Start date
2026-07-25
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Diseases requiring painless gastroenteroscopy examination include abdominal pain, hematochezia, anemia, gastrointestinal tumors, esophageal foreign bodies and other related conditions.

Interventions

R1 Group:Remimazolam 0.10 mg/kg was administered, followed by propofol at the corresponding dose to initiate the sequential trial.
R2 Group:Remimazolam 0.20mg/kg was administered, followed by propofol at the corresponding dose to initiate the sequential trial.
R3 Group:Remimazolam 0.2mg/kg was administered, followed by propofol at the corresponding dose to initiate the sequential trial.
R5 Group:Remimazolam 0.30mg/kg was administered, followed by propofol at the corresponding dose to initiate the sequential trial.
R4 Group:Remimazolam 0.25mg/kg was administered, followed by propofol at the corresponding dose to initiate the sequential trial.

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18–65 years, BMI 18–30 kg/m^2; 2.ASA physical status II–III; 3. Patients scheduled for painless gastrointestinal endoscopy; 4.Signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with severe cardiac, hepatic, renal or pulmonary dysfunction; 2. Patients with a preoperative history of alcoholism, opioid abuse or abuse of other sedatives; 3. Patients with upper respiratory tract infection within 2 weeks, difficult airway (Mallampati classification >= Grade III) or obstructive sleep apnea syndrome;

Design outcomes

Primary

MeasureTime frame
50% effective dose,ED50;95% effective dose,ED95;95%confidence interval,95%CI;

Secondary

MeasureTime frame
Mean Arterial Pressure (MAP);Bispectral Index(BIS);Heart Rart;Peripheral Oxygen Saturation(SpO2);

Countries

China

Contacts

Public ContactYue Lihui

Hebei General Hospital

13785123527@163.com+86 10 85988255

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026