Skip to content

Evaluation of the effect of remimazolam tosylate on anesthesia for prostate biopsy in the elderly

Evaluation of the effect of remimazolam tosylate on anesthesia for prostate biopsy in the elderly

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091993
Enrollment
Unknown
Registered
2024-11-07
Start date
2024-11-30
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Prostate puncture

Interventions

Remimazolam Tosylate Group:Remimazolam tosylate for anesthesia induction
Etomidate group:Etomidate for anesthesia induction

Sponsors

The First Affiliated Hospital of Xi'an Jiaotong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1.Age 65-85 years old; 2.NYHA heart function class I-II; 3.18kg/m^2<=BMI<=30kg/m^2 4.ASA classification I-III; 5.The patients and their families understood this study, voluntarily participated in this trial, and signed a written informed consent;

Exclusion criteria

Exclusion criteria: 1.Allergic to remimazolam tosylate or etomidate; 2.Severe renal insufficiency (dialysis required before surgery); 3.Severe liver impairment; 4.Patients with a history of mental and neurological diseases: such as depression, Parkinson's disease, basal ganglia lesions, schizophrenia, epilepsy, Alzheimer's disease, myasthenia gravis, cerebrovascular accident, etc.; 5.Patients who are considered unsuitable to participate in this trial by the researchers; 6.Participated in another study within 4 weeks before the current trial; 7.Patients with drug and alcohol abuse.

Design outcomes

Primary

MeasureTime frame
Postoperative recovery time;

Secondary

MeasureTime frame
Vital signs at different times, HR, MAP, SpO2, BIS values;Time to successful induction of anesthesia;Incidence of respiratory depression;Incidence of hypotension;Incidence of injection pain;Incidence of agitation during the awakening period;Incidence of nausea and vomiting;

Countries

China

Contacts

Public ContactYaomin Zhu

The First Affiliated Hospital of Xi'an Jiaotong University

zhuyaomin_mzk@163.com+86 18629382846

Outcome results

None listed

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