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Comparison of anesthetic effects of different doses of ketamine combined with propofol in hysteroscopic surgery

Comparison of anesthetic effects of different doses of ketamine combined with propofol in hysteroscopic surgery

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079740
Enrollment
Unknown
Registered
2024-01-11
Start date
2024-01-15
Completion date
Unknown
Last updated
2024-01-14

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

Conditions

Diseases undergoing hysteroscopic surgery

Interventions

Group K1:The patients were given 0.2 mg/kg ketamine combined with 2 mg/kg propofol intravenously and propofol 5 mg/kg/h by pump
Group K2:The patients were given 0.3 mg/kg ketamine combined with 2 mg/kg propofol intravenously and propofol 5 mg/kg/h by pump
Group K3:The patients were given 0.4 mg/kg ketamine combined with 2 mg/kg propofol intravenously and propofol 5 mg/kg/h by pump
Group K4:The patients were given 0.5 mg/kg ketamine combined with 2 mg/kg propofol intravenously and propofol 5 mg/kg/h by pump

Sponsors

Beijing Pinggu Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: Hysteroscopic surgery (including curettage, induced abortion and curettage) ; aged 18-70 years; Asa Grade I-II; Sign the informed consent form

Exclusion criteria

Exclusion criteria: ?severe diseases of important organs such as heart, lung and brain;? allergic reaction to ketamine and propofol;?severe arrhythmia; ? suspected or long-term use of narcotic drugs and psychotropic drugs;?severe hypertension, high intracranial pressure or hyperthyroidism

Design outcomes

Primary

MeasureTime frame
Incidence of ambulatory salvage propofol;

Secondary

MeasureTime frame
MAP, HR, SpO2 at 5 min before anesthesia (t0), when eyelash reflex disappeared (T1), when uterus was enlarged (T2), when surgery was closed (T3) and when awake (T4).;Awakening time, operation time, total propofol dosage and propofol dosage of patients in four groups.;Perioperative adverse reactions of four groups of patients;Classification of uterine contraction pain degree and improved Aldrete score in the four groups at 5, 15 and 30 min after awakening.;Likert satisfaction score of patients and operators in four groups;

Countries

China

Contacts

Public ContactZhang Zhijia

Beijing Pinggu Hospital

zhangzhijia727@126.com+86 158 1026 0002

Outcome results

None listed

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