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Clinical study on dose exploration of remifentanil tosylate in general anesthesia combined with iliac fascia block

Clinical study on dose exploration of remifentanil tosylate in general anesthesia combined with iliac fascia block

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500113569
Enrollment
Unknown
Registered
2025-12-01
Start date
2025-12-01
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Elderly Hip Replacement

Interventions

Group A Remimazolam Tosilate 0.2mg/kg/h:Administering different doses of remimazolam tobramate for anesthetic maintenance (0.2mg/kg/h)
Group B Remimazolam Tosilate 0.4mg/kg/h:Administering different doses of remimazolam tobramate for anesthetic maintenance (0.4mg/kg/h)
Group C Remimazolam Tosilate 0.6mg/kg/h:Administering different doses of remimazolam tobramate for anesthetic maintenance (0.6mg/kg/h)

Sponsors

Affiliated Hospital of Guizhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Patients scheduled for elective hip replacement surgery in the elderly 2) Patients aged 60 to 80 years 3) Patients with American Society of Anesthesiologists (ASA) physical status classification II to III 4) Patients with a Body Mass Index (BMI) between 18.5 and 23.9 kg/m² 5) Patients who voluntarily sign an informed consent form

Exclusion criteria

Exclusion criteria: 1) Patients known to be allergic to anesthetic drugs used in this study 2) Patients with myasthenia gravis, schizophrenia, and severe depressive states 3) Patients with concurrent severe malignant tumors, hematological diseases, and impaired liver or kidney function 4) Patients with obvious circulatory and respiratory dysfunction 5) Patients expected to be admitted to the ICU after surgery 6) Patients with an MMSE score <18 7) Patients who have received benzodiazepine treatment or participated in other clinical studies within the past 3 months

Design outcomes

Primary

MeasureTime frame
Intraoperative hemodynamic change indicators (MAP, HR);

Secondary

MeasureTime frame
Occurrence of low blood pressure;Average arterial pressure and HR of patients at different time points;

Countries

China

Contacts

Public ContactJinli Wu

Affiliated Hospital of Guizhou Medical University

jerry2021zheng@163.com+86 189 8510 0136

Outcome results

None listed

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