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Effects of Ciprofol on Hemodynamics and Postoperative Recovery Quality in Frail Patients Undergoing Holmium Laser Lithotripsy

Effects of Ciprofol on Hemodynamics and Postoperative Recovery Quality in Frail Patients Undergoing Holmium Laser Lithotripsy

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600119750
Enrollment
Unknown
Registered
2026-03-03
Start date
2026-03-03
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Holmium Laser Lithotripsy

Interventions

Ciprofol group:Anesthesia induction: Administer sufentanil 0.2–0.4 µg/kg, propofol 0.3–0.4 mg/kg, and rocuronium 0.6 mg/kg intravenously in sequence. Tracheal intubation or laryngeal mask insertion is
Propofol group:Anesthesia induction: Administer sufentanil 0.2–0.4 µg/kg, propofol 1.5–2.5 mg/kg, and rocuronium 0.6 mg/kg intravenously in sequence. Perform tracheal intubation or laryngeal mask inse
intraoperative circulation management and postoperative handling are the same as the cyclopropane propofol group.

Sponsors

Department of Anesthesiology, The First Affiliated Hospital of Henan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >=18 years, planned to undergo elective transurethral holmium laser lithotripsy; 2. Meet the diagnostic criteria for frailty (modified frailty index mFI >=0.27); 3. ASA classification II~IV; 4. Body mass index (BMI) 18~30 kg/m^2; 5. No contraindications to general anesthesia; 6. Clearly understand the study content and voluntarily participate in this study, signing the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Allergy to propofol, propofol-lipid formulations, or drugs related to this study (such as sufentanil, rocuronium, etc.); 2. Severe heart, lung, liver, or kidney dysfunction (Child-Pugh class C, eGFR =1 month); 5. Combined with cranial injury or intracranial hypertension; 6. Unable to cooperate with cognitive assessment or having communication disorders; 7. Expected surgery time 2 hours.

Design outcomes

Primary

MeasureTime frame
Blood Pressure;Postoperative Recovery Quality;Heart Rate;

Secondary

MeasureTime frame
Oxygen Saturation;Bispectral Index value;

Countries

China

Contacts

Public ContactYing Wang

The First Affiliated Hospital of Henan University

hdyfywy@163.com+86 138 3999 8369

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026