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Effects of different dosages of ketamine combined with ciprofol on laryngeal mask airway implantation under general anesthesia

Effects of different dosages of ketamine combined with ciprofol on laryngeal mask airway implantation under general anesthesia

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400080639
Enrollment
Unknown
Registered
2024-02-04
Start date
2024-02-05
Completion date
Unknown
Last updated
2024-02-05

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

Conditions

no limit

Interventions

K1: Anesthesia was induced by intravenous injection of penehyclidine 0.5 mg, midazolam 0.04 mg/kg, cisatracurium 0.2 mg/kg, sufentanil 0.2 µg/kg, corresponding doses of ketamine 0.2 mg/kg group and ci
K2: Anesthesia was induced by intravenous injection of penehyclidine 0.5 mg, midazolam 0.04 mg/kg, cisatracurium 0.2 mg/kg, sufentanil 0.2 µg/kg, corresponding doses of ketamine 0.3 mg/kg group and ci
k3: Anesthesia was induced by intravenous injection of penehyclidine 0.5 mg, midazolam 0.04 mg/kg, cisatracurium 0.2 mg/kg, sufentanil 0.2 µg/kg, corresponding doses of ketamine 0.4 mg/kg group and ci

Sponsors

The first affiliated hospital of henan university of CM
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1)Can understand and sign informed consent forms, (2) aged 18-60 years, (3)ASA is classified as Grade I or II (4) BMI 18-28 kg/m^2, (5)There is no allergy or intolerance to the research medication; (6) general anesthesia with laryngeal mask airway (LMA) , (7)Not involved in other clinical studies.

Exclusion criteria

Exclusion criteria: (1) pregnant women, (2) history of asthma, (3) alcohol abuse, (4) heart, liver and kidney dysfunction, (5) patients with mental disorders and communication disorders, (6) patients with poorly controlled or untreated hypertension; (7) Patients who have taken psychiatric or opioid drugs intermittently within the past 3 months or continuously within 1 month.

Design outcomes

Primary

MeasureTime frame
Hart rate;

Secondary

MeasureTime frame
Mean arterial pressure;The occurrence of body movements and laryngeal spasms;Rating of ease of placement of laryngeal mask;VAS pain score;

Countries

China

Contacts

Public ContactZhang Yi

No.19 Renmin Road, Zhengzhou City, Henan Province

290364006@qq.com+86 155 1753 3365

Outcome results

None listed

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