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Clarify the advantages of using remimazolam besylate in reducing perioperative adverse reactions during general anesthesia for elderly orthopedic surgery

Clinical Research on the Remimazolam Besylate for Injection in Elderly Patients Undergoing General Anesthesia for Orthopedic Surgery.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128319
Enrollment
Unknown
Registered
2026-07-17
Start date
2026-01-05
Completion date
Unknown
Last updated
2026-07-20

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

Conditions

Postoperative delirium

Interventions

Group C: Remimazolam-induced maintenance group:Anesthesia induction and maintenance with remazolam besylate
Group B: Remimazolam-induced sevoflurane maintenance group
:Anesthesia induction with remazolam besylate and maintenance with sevoflurane
Group A: Etomidate induction, sevoflurane maintenance group
:Etomidate anesthesia induction and sevoflurane maintenance

Sponsors

Sichuan Provincial Orthopaedic Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. The clinical data of the patients are accurate and complete in terms of collection and preservation. 2. There is no gender restriction. The age>= 65 years old, and BMI in the range of 18-30 kg/m^2. 3. The preoperative American Society of Anesthesiologists (ASA) classification should be grade I - III, and Mallampati airway classification should be grade I - III. 4.The operation time should be more than 0.5 hours. 5.The patients should have clearly understood the content of this study before the operation and voluntarily participated, and have signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients who have been using psychotropic drugs and sedative and analgesic drugs for a long time, or those who are allergic to the study drugs or have contraindications for their use; 2. Patients with severe diseases of the circulatory system, respiratory system, endocrine system and liver-kidney functions; 3. Patients with abnormal cognitive function and communication disorders; 4. Patients who have unexpected events requiring emergency treatment during the operation, such as severe drug allergy, arrhythmia, etc., with operation time longer than 3 hours or blood loss more than 200 ml; 5.Patients who use sedative drugs after the operation.

Design outcomes

Primary

MeasureTime frame
Hemodynamic indicators;The prevalence of postoperative delirium;

Secondary

MeasureTime frame
VAS score;QoR-40 Scale;Lipoprotein-associated phospholipaseA2 (Lp-PLA2);QoR-40 Scale;Central nervous system specific protein ß (S100ß);

Countries

China

Contacts

Public ContactPeiyu Li

Sichuan Provincial Orthopaedic Hospital

65223091@qq.com+86 18215526780

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026