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The effective dose of ciprofol combined with low-dose sufentanil to inhibit uterine dilation reaction

The effective dose of ciprofol combined with low-dose sufentanil to inhibit uterine dilation reaction

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065954
Enrollment
Unknown
Registered
2022-11-19
Start date
2022-11-19
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Diseases requiring hysteroscopy

Interventions

Group H:Intravenous ciprofol
Group B:Intravenous propofol

Sponsors

Obstetrics and Gynecology Hospital Affiliated to Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: 1. Patients undergoing elective hysteroscopy; 2. Aged 18-64 years, BMI 18-25 kg/m2; 3. ASA grade I-II.

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating women; 2. There are contraindications to routine hysteroscopy; 3. Cyclopofol and propofol are contraindicated; 4. A history of mental illness; 5. Complicated with severe cardiopulmonary disease; 6. Use analgesics within 24 hours before surgery; 7. Patients who are participating in other clinical studies; 8. The researchers believe that other reasons are not suitable for clinical researchers.

Design outcomes

Primary

MeasureTime frame
Whether there is a positive reaction;

Secondary

MeasureTime frame
Systolic blood pressure, SBP;Mean arterial pressure, MAP;Heart rate, HR;Pulse oxygen saturation, SpO2;Respiratory rate, RR;Pressure of end-tidal carbon dioxide, ETCO2;Entropy index;Surgical pleth index, SPI;Adverse reactions;

Countries

China

Contacts

Public ContactXinzhong Chen

Obstetrics and Gynecology Hospital Affiliated to Zhejiang University School of Medicine

m18334532797@163.com+86 18334532797

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 5, 2026