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A Comparative Study on Postoperative Recovery Quality Between Remimazolam Tosylate and Propofol in Patients with Hidden Obesity Undergoing General Anesthesia for Unilateral Biportal Endoscopic Surgery

A Comparative Study on Postoperative Recovery Quality Between Remimazolam Tosylate and Propofol in Patients with Hidden Obesity Undergoing General Anesthesia for Unilateral Biportal Endoscopic Surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600125190
Enrollment
Unknown
Registered
2026-05-22
Start date
2026-05-25
Completion date
Unknown
Last updated
2026-05-25

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

Conditions

None

Interventions

Remimazolam Tosylate Group:General anesthesia with remimazolam tosylate

Sponsors

The First Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18-65 years, regardless of gender 2. Normal BMI (18.5-23.9 kg/m²) but meeting one of the hidden obesity diagnostic criteria: Body fat percentage: male >=20%, female >=30% Waist-to-hip ratio: male >0.9, female >0.85 Visceral fat area: male >=100 cm², female >=80 cm² 3. Elective unilateral biportal endoscopic (UBE) surgery with anesthesia duration <=2 hours 4. ASA physical status class ?-? 5. Signed informed consent

Exclusion criteria

Exclusion criteria: 1. Allergy to propofol emulsifier (soybean lecithin) or remimazolam 2. History of epilepsy or convulsions 3. Pregnant or breastfeeding women 4. Uncontrolled hypertension (systolic BP>160 mmHg or diastolic BP>100 mmHg) 5. Severe cardiopulmonary diseases (e.g., myocardial infarction, heart failure, acute asthma exacerbation) 6. Severe hepatic or renal insufficiency (Child-Pugh class C, Cr>2 mg/dL) 7. Coagulation disorders (INR>1.5, platelet count2 hours 11. Recent use of CYP3A4 inhibitors (e.g., ketoconazole) or diuretics 12. Preoperative acute infection or inflammation

Design outcomes

Primary

MeasureTime frame
Extubation time (spontaneous breathing recovery with SpO2 >= 95%);

Secondary

MeasureTime frame
Anesthesia maintenance stability;Postoperative 24-hour pain VAS score;Postoperative 24-hour patient satisfaction;Incidence of postoperative nausea and vomiting (PONV);Incidence of hypoxemia;

Countries

China

Contacts

Public ContactYan Wei

The First Affiliated Hospital of Harbin Medical University

31660213@qq.com+86 139 3626 1086

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026