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Hemodynamic Effects (CI/SVR) of Ciprofol vs. Propofol during Anesthesia Induction in Older Orthopedic Patients: A Randomized Controlled Study

Hemodynamic Effects (CI/SVR) of Ciprofol vs. Propofol during Anesthesia Induction in Older Orthopedic Patients: A Randomized Controlled Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500114091
Enrollment
Unknown
Registered
2025-12-08
Start date
2025-12-10
Completion date
Unknown
Last updated
2025-12-15

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

Conditions

?Hemodynamic Instability

Interventions

Cipepofol Group (C):1. Anesthesia induction: intravenous bolus of propofol 0.4 mg/kg (injected over >=60 seconds). 2. Anesthesia maintenance: continuous intravenous infusion of propofol, with dosage
continuous intraoperative infusion of remifentanil, with additional sufentanil and/or cisatracurium administered as needed.
Propofol Group (P) :1. Anesthesia Induction: Intravenous (IV) bolus of Propofol 2.0 mg/kg (injection time >=60 seconds). 2. Anesthesia Maintenance: Continuous IV infusion of Propofol, with the dose ti
continuous infusion of Remifentanil during surgery, with supplemental doses of Sufentanil and/or Cisatracurium administered as needed. (Identical to the Ciprofol Group)

Sponsors

The First Affiliated Hospital of USTC (Anhui Provincial Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age 60-75 years, no restriction on gender; 2. ASA classification I-III, without cardiovascular complications; 3. Scheduled for elective orthopedic joint (knee/hip) replacement surgery under general anesthesia (expected surgery duration between 1 and 3 hours); 4. BMI at enrollment between 18-30 kg/m^2; 5. Able to understand the study and provide informed consent.

Exclusion criteria

Exclusion criteria: 1. Allergy to propofol, soybean, or eggs; 2. Uncontrolled hypertension (systolic BP >=180 mmHg or diastolic BP >=110 mmHg) or preoperative hypotension (MAP 40 g/day) or opioid dependence.

Design outcomes

Primary

MeasureTime frame
Cardiac Index (CI);Systemic Vascular Resistance (SVR);

Secondary

MeasureTime frame
Mean Arterial Pressure (MAP);Incidence of Hypotension;the dose of vasopressor;Time to Loss of Consciousness (LOC);BIS Value;total consumption of anesthetic ;Extubation Time;

Countries

China

Contacts

Public ContactGuo Fenglin

The First Affiliated Hospital of USTC (Anhui Provincial Hospital)

1030651261@qq.com+86 153 9500 6763

Outcome results

None listed

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