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Comparing the vasodilatory properties of Ciprofol and propofol at ED50 doses using perfusion index

Comparing the vasodilatory properties of Ciprofol and propofol at ED50 doses using perfusion index

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127001
Enrollment
Unknown
Registered
2026-06-22
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Intraoperative hemodynamic disturbance during gynecological surgery

Interventions

Group A: Ciprofol group in Phase 1:The initial dose of ciprofol was 0.4 mg/kg, administered as a uniform intravenous bolus over 30 seconds. The dose step for the ciprofol group was 0.05 mg/kg. The tri
Group B: Propofol group in Phase 1:The initial dose of propofol was 1.5 mg/kg, administered via intravenous bolus at a constant rate over 30 seconds. The dose step for the propofol group was 0.25 mg/k
Group C: Ciprofol group in Phase 2:Both groups were given the ED50 determined in Phase1 via uniform intravenous injection over 30 seconds. PI, MAP and HR were recorded at 1 min, 2 min and 3 min after
Group P: Propofol group in Phase 2:Both groups were given the ED50 determined in Phase1 via uniform intravenous injection over 30 seconds. PI, MAP and HR were recorded at 1 min, 2 min and 3 min after

Sponsors

The Third Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
22 Years to 45 Years

Inclusion criteria

Inclusion criteria: 1. Female patients aged 22 to 45 years. 2. Scheduled for elective gynecological surgery under general anesthesia. 3. ASA physical status class ?–?. 4. Body mass index (BMI): 18–28 kg/m².

Exclusion criteria

Exclusion criteria: 1.Patients with allergy to ciprofol, propofol or their ingredients. 2.Patients complicated with cardiovascular diseases or peripheral vascular diseases (e.g., Raynaud's syndrome). 3.Anemia (Hb < 90 g/L) or hypoalbuminemia (albumin < 30 g/L). 4.Preoperative use of vasoactive drugs, calcium channel blockers, ß-receptor blockers or anticholinergic agents. 5.History of diabetes mellitus, neurological or psychiatric disorders. 6.Abnormal hepatic and renal function. 7.History of drug abuse, anxiety or depression. 8.Fingernail polish on the monitored finger, abnormal skin temperature or peripheral circulatory disorders.

Design outcomes

Primary

MeasureTime frame
Perfusion index (PI) at 1, 2, and 3 minutes after administration, and the rate of change of PI.;ED50 of Ciprofol and Propofol.;

Secondary

MeasureTime frame
Mean arterial pressure;Heart rate;

Countries

China

Contacts

Public ContactJi Leting

The Third Affiliated Hospital of Zhengzhou University

jlt0001@126.com+86 185 3800 6729

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 3, 2026