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Comparative study of Remazolam besylate, cyclopofol and propofol combined with low-dose sufentanil in hysteroscopic surgery

Comparative study of Remazolam besylate, cyclopofol and propofol combined with low-dose sufentanil in hysteroscopic surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300069105
Enrollment
Unknown
Registered
2023-03-07
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-05-22

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

Conditions

Comparative study of Remazolam besylate, cyclopofol and propofol combined with low-dose sufentanil in hysteroscopic surgery

Interventions

group R:Anesthesia induction: Remazolam besylate 0.2mg/kg+ sufentanil 0.1ug/kg Maintenance of anesthesia: Remazolam besylate 1mg/kg/h
group H:Anesthesia induction: cipofol 0.4mg+ sufentanil 0.1ug/kg Anesthesia maintenance: cipofol 8mg/kg/h
group P:Anesthesia induction: propofol 2mg/kg+ sufentanil 0.1ug/kg Anesthesia maintenance: propofol 8mg/kg/h

Sponsors

Lishui People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ? They all meet the standard of hysteroscopic surgery; ? Female aged 18-65 ? No allergy to the anesthetic ingredients used in the study; ?ASA grading is I~II; ?BMI 18-28 kg/? ? Normal mind, able to cooperate with surgery; ? Volunteer to participate in this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: ? Combined with malignant tumor; ? Weak body, unable to tolerate surgery; ? Complicated with serious heart, liver and kidney system diseases; ? Pregnancy and lactation; ? Known or suspected to be allergic or contraindicated to various components of the study drug or other benzodiazepines, opioids, propofol, etc; ? Those who have participated in any clinical trial as subjects within 3 months before enrollment; ? Incomplete clinical data ? Other conditions determined by the researcher to be unsuitable for selection.

Design outcomes

Primary

MeasureTime frame
blood pressure;oxygen saturation;heart rate;Rate of respiration;

Secondary

MeasureTime frame
Modified Observer's assessment alert/Sedation;wake up of time;Adverse reaction rate;

Countries

China

Contacts

Public ContactWeifeng Shan

Lishui People's Hospital

Shanweifeng@163.com13516805847

Outcome results

None listed

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