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Application of intravenous remimazolam in hysteroscopic surgery

Application of intravenous remimazolam in hysteroscopic surgery

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300067819
Enrollment
Unknown
Registered
2023-01-28
Start date
2023-01-28
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Endometrial disease

Interventions

Group 1:Remimazolam 0 mg/kg
Group 2:Remimazolam 0.5 mg/kg
Group 3:Remimazolam 1.0 mg/kg
Group 4:Remimazolam 1.5 mg/kg
Group 5:Remimazolam 2.0 mg/kg

Sponsors

Women’s Hospital, Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing hysteroscopic surgery under intravenous anesthesia; 2. ASA grade I-II, aged 18-55 years, BMI 18-24 kg/m2; 3. No electrolyte disorder, infection, immune and endocrine system diseases, no recent use of cardiovascular drugs, non-steroidal anti-inflammatory drugs, hormone drugs and anti-psychotic drugs.

Exclusion criteria

Exclusion criteria: 1. Previous history of vaginal birth; 2. Abnormal liver and kidney function; 3. History of cardiopulmonary diseases; 4. Sleep apnea syndrome; 5. Long-term use of drugs such as diazepam; 6. Long-term users of opioids; 7. People allergic to remimazolam.

Design outcomes

Primary

MeasureTime frame
propofol effective concentration 50 (EC50);

Secondary

MeasureTime frame
Intraoperative vital signs;The recovery time;Adverse reactions;

Countries

China

Contacts

Public ContactXinzhong Chen

Women’s Hospital, Zhejiang University School of Medicine

chenxinz@zju.edu.cn+86 18806523402

Outcome results

None listed

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