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The effect of sedation with dexmedetomidine on the incidence of delirium after spinal anesthesia in elderly patients with hip surgery

The effect of sedation with dexmedetomidine on the incidence of delirium after spinal anesthesia in elderly patients with hip surgery

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0003133
Enrollment
110
Registered
2018-08-28
Start date
2018-07-16
Completion date
Unknown
Last updated
2021-07-12

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

Conditions

None listed

Interventions

Drug : Dexmedetomidine was administered at a dose of 1 mcg / kg for 10 minutes via intravenous line. and then 0.2 mcg / kg / hr administration via intravenous line till the end of surgery. Only the sp

Sponsors

Yonsei University, Wonju Severance Christian Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: - Patients scheduled to undergo a 65-year-old hip replacement with scheduled spinal anesthesia - American Society of Anesthesiology grade 1,2,3 patients

Exclusion criteria

Exclusion criteria: - Under 65 - American society of Anesthesiology grade 4 or higher - People who take Nore epinephrine reuptake inhibitors. (Eg tricyclic antidepressants, monoamine oxidation inhibitors, acute cocaine intoxication) - myocardial infarction and stroke within the past one year - Prior to major cardiac surgery within 1 year - Patients who require vasodilators or oxygen therapy because they are anxious before surgery. - Patients with fever (> 38 degrees) - Patients with a history of drug hypersensitivity prior to sedation. - Uncontrolled hypertension - Patients who can not talk and have cognitive impairment - Patients with a history of mental illness - Brain damage, neurosurgical surgery. - Preoperative Ejection fraction less than 30%, or a person with a heart rhythm disorder (Sick sinus syndrome, bradycardia less than 50 beats per minute, 2 or more degrees of atriovanetricular block without artificial heart rhythm. - A patient with severe liver disease of Child-Pugh class C or higher. - renal dysfunction with dialysis - If the subject includes a person who can not read the consent form (eg, illiterate, foreigner, etc.) - a patient have received other treatment or surgery. - Those who have less chance of survival than 24 hours.

Design outcomes

Primary

MeasureTime frame
frequency of postoperative delirium

Secondary

MeasureTime frame
the amount of bleeding

Countries

Korea, Republic of

Contacts

Public ContactJi Hyoung Park

Yonsei University, Wonju Severance Christian Hospital

killerjhjh@naver.com+82-33-741-1604

Outcome results

None listed

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