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Efficacy of remimazolam besylate versus propofol plus remifentanil for maintenance of anesthesia in elderly patients: a randomized controlled trial

Efficacy of remimazolam besylate versus propofol plus remifentanil for maintenance of anesthesia in elderly patients: a randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074156
Enrollment
Unknown
Registered
2023-07-31
Start date
2023-08-01
Completion date
Unknown
Last updated
2023-08-07

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

Conditions

Prostatic hyperplasia, delirium, nausea and vomiting

Interventions

Remazolam group (R group):Anesthesia induction and maintenance were performed with remimazolam as the leading agent
(P):Anesthesia induction and maintenance were performed with propofol as the leading agent

Sponsors

Deyang People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1: age = 65 years old 2: American Society of Anesthesiologists Grade ?III 3: Patients undergoing elective transurethral resection of prostate

Exclusion criteria

Exclusion criteria: 1: patients with long-term benzodiazepine and opioid addiction 2: ASA> III, patients with poorly controlled severe cardiovascular and cerebrovascular disease (history of cerebrovascular accident, myocardial infarction, or unstable angina within 3 months, and preoperative blood pressure of 180/110 mmHg or above) 3: patients with drug allergy related to the study 4: patients with preoperative cognitive impairment and psycho-physical and psychiatric disorders 5: patients with preoperative cognitive impairment 6:Patient with severe liver and kidney dysfunction: BMI26.9 7: Patients with myasthenia gravis

Design outcomes

Primary

MeasureTime frame
Time to recovery from anesthesia or time to removal of laryngeal mask;Induction time of anesthesia;Heart rate, blood pressure;

Secondary

MeasureTime frame
Postoperative VAS pain score;delirium;Resuscitation room stay time;Respiratory depression, nausea and vomiting;intraoperative awareness;Catheter-related bladder discomfort;

Countries

China

Contacts

Public ContactChao Xiong

Deyang People's Hospital

15808485903@163.com+86 158 0848 5903

Outcome results

None listed

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