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A study on the application of cyclopofol combined with nalbuphine in laryngeal mask general anesthesia for day hysteroscopic surgery

A study on the application of cyclopofol combined with nalbuphine in laryngeal mask general anesthesia for day hysteroscopic surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079340
Enrollment
Unknown
Registered
2024-01-01
Start date
2024-01-01
Completion date
Unknown
Last updated
2024-01-08

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

Conditions

Uterine cavity vegetations

Interventions

A (cyclopofol 0.4 mg/kg + nalbuphine ED95) :Group A was given nalbuphine ED95, followed by cyclopofol 0.4mg/kg, and a laryngeal mask was placed when the patient s eyelash reflex disappeared and the Na
B (cyclopofol 0.4 mg/kg + sufentanil 0.1 µg/kg) 2:Group B was given sufentanil 0.1 µg/kg, then cyclopofol 0.4 mg/kg, and when the patient s eyelash reflex disappeared, the laryngeal mask was placed wh

Sponsors

The First People's Hospital of Jingzhou City
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Age 18~60 years old, ASA classification I.~II., BMI 18.0~28.0kg/m2, Mallampati grade I or II, mouth opening > 2.5cm, no airway abnormality, no long-term use of sedative-hypnotic drugs, history of alcohol dependence.

Exclusion criteria

Exclusion criteria: Those who refuse to participate or are not suitable to participate in this trial; Those who are clearly allergic to cyclopofol or nalbuphine; Patients with severe cardiovascular disease, severe diabetes mellitus, hyperkalemia, liver and kidney dysfunction or impaired adrenal cortical function; Patients with central nervous system disease, difficult airway, and acute upper respiratory tract infection; Previous use of sedative-hypnotic drugs, history of drug or alcohol dependence; History of alcohol abuse or taking psychotropic drugs or analgesic drugs within 24 hours before surgery; Patients with severe visual or hearing impairment or who are unable to communicate with the visitor or refuse to communicate for other reasons; history of psychological problems or psychiatric illness; Pregnancy or lactation.

Design outcomes

Primary

MeasureTime frame
Laryngeal mask placement reaction;

Secondary

MeasureTime frame
The HR, SBP, DBP, MAP, and Narcotrend indices were used at six time points before administration (T0), 1 min after administration (T1), 1 minute after laryngeal mask insertion, 5 min (T3), hysteroscopy into the uterine cavity (T4), and at the end of surgery (T5).;

Countries

China

Contacts

Public ContactYi Chen

The First People's Hospital of Jingzhou City

591938696@qq.com+86 181 6313 8558

Outcome results

None listed

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