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The Dose Range of Remimazolam Besylate in Different Age Groups

The Investigation of the Dose Range of Remimazolam Besylate in Different Age Groups of Adults and Its Effects on Hemodynamics

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06009991
Enrollment
1876
Registered
2023-08-24
Start date
2023-07-17
Completion date
2025-12-31
Last updated
2023-09-06

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

Conditions

Anesthesia, Remimazolam

Brief summary

This is a multicenter, randomized, parallel, controlled clinical study of patients at different ages underwent elective non-cardiac surgery under general anesthesia. The aim of this study is to explore the dose range of remimazolam besylate for patients at different ages, to provide guidance for anesthesia induction and maintenance of remimazolam besylate. And to investigate the incidence of perioperative hypotension and postoperative related organ dysfunction in patients received total intravenous anesthesia with remimazolam besylate, compared with propofol.

Detailed description

Surgery is an effective method to treat surgical diseases, prolong survival time and improve the quality of life, but patients often face the risk of postoperative complications. In general surgery patients, complications occur in more than 30% of patients. Several observational studies have shown that the severity and duration of intraoperative hypotension are significantly related to the risk of postoperative adverse events such as myocardial injury, renal injury, stroke, delirium, prolonged hospitalization, and death. Hypotension, defined as a systolic blood pressure of less than 90 mmHg, a diastolic blood pressure of less than 50 mmHg, or a 20% reduction in systolic blood pressure from baseline, is common during anesthesia and surgery. More than a third of patients receiving propofol sedation experience intraoperative hypotension events, and their duration and degree are associated with harm during surgery. Remimazolam is a new ultra-short-acting sedative drug developed in recent years, which has a similar structure to midazolam. However, compared with midazolam, remimazolam has the advantages of faster onset, faster recovery, and higher safety. Compared with propofol, remimazolam is noninferior in the success rate of sedation, while the incidence of adverse events such as hypotension is lower. At present, remimazolam has completed phase III clinical studies in many fields, such as colonoscopy, fiberoptic bronchoscopy, and general anesthesia induction and maintenance, which have shown its safety and effectiveness. However, there may be differences in hemodynamics and drug sensitivity among patients of different ages. Compared with young patients, elderly patients have a higher risk of hypotension after anesthesia induction. At present, there is a lack of clinical studies with large samples to clarify the recommended dose of remimazolam for anesthesia induction and maintenance in patients of all ages. The updated instructions for remimazolam besylate for injection on March 28, 2022 also mention that remimazolam besylate is used as a sedative drug for general anesthesia induction and maintenance, and the relevant dose reference is given. However, the safety and effectiveness of patients over 65 years have not been confirmed. The precise regulation of clinical use for patients of different ages and the optimization of drug dosage during anesthesia induction and maintenance are the basis for ensuring the safety of clinical medication at present., in order to maintain the stability of perioperative hemodynamics, and prevent or reduce the occurrence of adverse cardiovascular events. This study aims to investigate the effect of remimazolam total intravenous anesthesia on intraoperative hemodynamics and the drug requirement for patients of different ages, with propofol as the control, and intraoperative hemodynamics as the main evaluation index, so as to provide evidence for clinical application of remimazolam for elderly patients in anesthesia induction and maintenance.

Interventions

DRUGRemimazolam besylate

Age 45-64: Remimazolam Besylate 0.3 mg/kg for anesthesia induction (0.05mg/kg for additional need) and 0.5mg/kg/h for maintenance (0.25 mg/kg/h for additional need). Age over 65: Remimazolam Besylate 0.15 mg/kg for anesthesia induction (0.05mg/kg for additional need) and 0.5mg/kg/h for maintenance (0.25 mg/kg/h for additional need).

DRUGPropofol

Age 45-64: Propofol 3.0μg/ml TCI for anesthesia induction and 2.5-3.0μg/ml TCI for maintenance. Age over 65: Propofol 1.5-2.5μg/ml TCI for anesthesia induction and 1.5-2.5μg/ml TCI for maintenance

Sponsors

Renmin Hospital of Wuhan University
CollaboratorOTHER
Wuhan University
CollaboratorOTHER
The General Hospital of Central Theater Command
CollaboratorOTHER
Taihe Hospital
CollaboratorOTHER
Yichang Central People's Hospital
CollaboratorOTHER
Jingzhou Central Hospital
CollaboratorOTHER
Beijing Shijitan Hospital, Capital Medical University
CollaboratorOTHER
The Affiliated Nanjing Drum Tower Hospital of Nanjing University Medical School
CollaboratorOTHER
First Affiliated Hospital of Fujian Medical University
CollaboratorOTHER
Tianjin Nankai Hospital
CollaboratorOTHER
Sichuan Provincial People's Hospital
CollaboratorOTHER
Shanxi Bethune Hospital
CollaboratorOTHER
Tongji Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
45 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. age above 45 years old; 2. American Society of Anesthesiologists grade Ⅰ-II; 3. patients undergoing tracheal intubation or laryngeal mask airway surgery under general anesthesia (intravenous anesthesia); 4. Informed consent: patients voluntarily participated in the trial and signed the informed consent form.

Exclusion criteria

1. patients with cardiac function grade 3 or above; 2. difficult to observe the pupil size of head or neck surgery patients; 3. patients with multimodal anesthesia such as nerve block or spinal anesthesia compounded; 4. patients known to be allergic to remimazolam besylate or benzodiazepines; 5. major vascular surgery and the type of surgery that directly affects hemodynamics; 6. patients with coagulation dysfunction, endocrine diseases or other hemodynamic conditions; 7. minor surgery (operation duration \<1 hour); 8. surgery lasting more than 4 hours; 9. emergency surgery; 10. patients with a history of drug or alcohol dependence; 11. Subjects deemed unsuitable for the study by the investigator.

Design outcomes

Primary

MeasureTime frameDescription
Occurrence of intraoperative hypotensionOperation 1 dayOccurrence of intraoperative hypotension

Secondary

MeasureTime frameDescription
Anesthesia recoveryOperation 1 dayAnesthesia recovery
Cognitive function assessmentOperation 1 dayCognitive function assessment in the anesthesia recovery room
Intraoperative dosage of vasoactive drugsOperation 1 dayIntraoperative dosage of vasoactive drugs
Hospital stay of patientsWith 30 days after surgeryHospital stay of patients
30-day mortality after surgery30-day after surgery30-day mortality after surgery
Major organ complicationsWithin 30 days after surgeryThe occurrence of major organ complications within 30 days after surgery

Countries

China

Contacts

Primary ContactQiaoqiao Xu
qiaoqiaoxu@aliyun.com+8618771006963

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026