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The effective dose of remimazolam combined with different doses of olanzapine fumarate in hysteroscopic examination surgery.

The effective dose of remimazolam combined with different doses of olanzapine fumarate in hysteroscopic examination surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094020
Enrollment
Unknown
Registered
2024-12-16
Start date
2024-12-23
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

None

Interventions

Remimazolam +0.02mg/kg oxalidine fumarate group:0.02mg/kg oliceridine+ remimazolam
Remimazolam +0.025mg/kg oxalidine fumarate group:0.025mg/kg oliceridine+ remimazolam

Sponsors

Affiliated Shunde Hospital of Jinan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 18 and 60 years old, with a body mass index (BMI) ranging from 18 to 28 kg/m², Mallampati grade ? or ?, and no abnormalities in airway, head and neck conditions. 2. American Society of Anesthesiologists (ASA) score of grade I or II. 3. Patients scheduled for hysteroscopy. 4. Patients volunteer to participate in this study. 5. Having not taken sedative and analgesic drugs recently, with no history of mental and neurological diseases, and no history of severe heart, lung, liver and kidney diseases.

Exclusion criteria

Exclusion criteria: 1.Patients who refused to participate or were not suitable to participate in this trial; 2.Those with contraindications for anesthesia and surgery; 3.Those who used anesthetic drugs, sedatives or opioid drugs within 24 hours before surgery; 4.Patients with myasthenia gravis; 5.Patients in a severe depressive state; 6.Those allergic to benzodiazepines; 7.Patients with liver and kidney dysfunction combined with endocrine and metabolic diseases; 8.Those accompanied by mental and neurological diseases; 9.Those without obtaining the informed consent of the patients; 10 Those with unstable vital signs due to various serious diseases.

Design outcomes

Primary

MeasureTime frame
Dose of remimazolam;

Secondary

MeasureTime frame
Heart rate;Breathing;Recovery time;Adverse reactions;

Countries

China

Contacts

Public ContactZheng Yuling

Affiliated Shunde Hospital of Jinan University

5271107@qq.com+86 137 9406 2538

Outcome results

None listed

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