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Efficacy and Safety of Oliceridine in Conjunction with Etomidate for Hysteroscopic Surgery

Study on the Efficacy and Safety of Oliceridine in Conjunction with Etomidate for Hysteroscopic Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114676
Enrollment
Unknown
Registered
2025-12-16
Start date
2024-10-01
Completion date
Unknown
Last updated
2026-01-05

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

Conditions

Gynecological disease

Interventions

Oxaliplatin-combined with rimegepant group:Oxelizine 0.03mg/kg intravenously
Sufentanil composite etomidate group:Intravenous infusion of sufentanil 0.10 µg/kg

Sponsors

Qingdao Women and Children's Hospital (Peking University People's Hospital Qingdao Hospital)
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Scheduled hysteroscopic surgery; 2. Age 18-60 years; 3. American Anesthesiologists Association (ASA) classification I-II; 4. Body mass index (BMI) 18-28 kg/m².

Exclusion criteria

Exclusion criteria: 1. History of liver, kidney, or cardiovascular disease; 2. Severe hypertension (systolic blood pressure >=180mmHg or diastolic blood pressure >=110mmHg), diabetes (random blood glucose >=11.1mmol/l or fasting blood glucose >=7mmol/l); 3. Concomitant central nervous system disease; 4. Obstructive airway; 5. Allergy to the investigational drug.

Design outcomes

Primary

MeasureTime frame
body movement;

Secondary

MeasureTime frame
Respiratory depression;Time to action of the two groups;hemodynamics;Total dose of etomidate;Recovery time of consciousness;

Countries

China

Contacts

Public ContactHan Long

Qingdao Women and Children's Hospital (Peking University People's Hospital Qingdao Hospital)

252628848@qq.com+86 185 5326 2213

Outcome results

None listed

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