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The Value of Remimazolam for General Anesthesia in Elderly Frail Patients Undergoing Transurethral Plasma Kinetic Enucleation of the Prostate

The Value of Remimazolam for General Anesthesia in Elderly Frail Patients Undergoing Transurethral Plasma Kinetic Enucleation of the Prostate

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111144
Enrollment
Unknown
Registered
2025-10-27
Start date
2025-11-01
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

benign prostatic hyperplasia

Interventions

Propofol Group :Anesthesia induction: Propofol
Anesthesia maintenance: Continuous infusion of propofol and remifentanil (analgesic)
Remimazolam Group:Anesthesia induction: Remimazolam
Anesthesia maintenance: Continuous infusion of Remimazolam and Remifentanil (analgesic)

Sponsors

Meishan People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. All meet the surgical indications for transurethral plasma resection of the prostate; 2. All are scheduled to undergo elective transurethral plasma resection of the prostate; 3. Age >= 65 years; 4. Quick frailty questionnaire (FRAIL) score >= 3 points; 5. All are planned to undergo general anesthesia; 6. Anesthesia classification II~III; 7. Patients and their families are informed about this study and have signed the consent form.

Exclusion criteria

Exclusion criteria: 1. Accompanied by cardiovascular diseases (coronary heart disease, arrhythmia, hypertension, etc.); 2. Accompanied by metabolic diseases (diabetes); 3. Accompanied by liver or kidney dysfunction, or coagulation disorders; 4. Accompanied by psychiatric disorders, unable to cooperate with the investigator; 5. History of dependence on sedatives or analgesics, and history of alcoholism; 6. Body mass index >30 kg/m^2; 7. History of prostate surgery; 8. Expected surgery duration >2 hours; 9. Allergy or intolerance to anesthetics used in this study; 10. Patients with myasthenia gravis.

Design outcomes

Primary

MeasureTime frame
Monitor vital sign fluctuations;

Secondary

MeasureTime frame
Onset and recovery of anesthesia;Cognitive function ;Adverse reaction;

Countries

China

Contacts

Public ContactLi Na

Meishan People's Hospital

267032219@qq.com+86 135 6830 3225

Outcome results

None listed

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