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Clinical observation of different induction schemes of general anesthesia in elderly patients

Clinical observation of different induction schemes of general anesthesia in elderly patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000040133
Enrollment
Unknown
Registered
2020-11-22
Start date
2020-12-01
Completion date
Unknown
Last updated
2021-01-11

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

Conditions

Elderly patients

Interventions

Sufentanil group (Group F, n = 20), group K1 (Group K1, n = 20), group K2 (Group K2, n = 20) and group 3 (Group K3, n = 20) were treated with sufentanil (Group F, n = 20), group K1 (Group K1, n = 20),

Sponsors

Tianjin Fourth Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) The patients aged 65 to 80 years old; patients who planned to undergo endotracheal intubation; ASA score of grade I or II or grade III; 2) BMI 18 to 30kg/m2; 3) They clearly understood and voluntarily participated in the study, and their informed consent was signed by themselves.

Exclusion criteria

Exclusion criteria: 1) Patients who refuse to participate or who are not suitable to participate in the trial; 2) Those who are sensitive to esmamine and related drugs; 3) In the past, there were contraindications for ketamine use, such as severe refractory hypertension, pulmonary heart disease, hyperthyroidism, epilepsy, increased intraocular pressure, intracranial space occupying lesions, and history of cerebrovascular accidents; 4) There was a history of alcoholism or taking psychotropic drugs or analgesics within 24 hours before operation; 5) Epileptic seizures; 6) Use drugs that affect the central nervous system; 7) He had a history of severe depression, mental and neurological diseases in the past. 8) The researchers believe that patients should not participate in the trial.

Design outcomes

Primary

MeasureTime frame
Efficacy evaluation;

Countries

China

Contacts

Public ContactMu Rong

Tianjin Fourth Central Hospital

yymurong@126.com+86 13752002295

Outcome results

None listed

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