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Comparison of delirium after knee replacement surgery in elderly patients with propofol and dexmedetomidine.

Comparison of the Incidence of Postoperative Delirium in Elderly Patients Over 60 Undergoing Knee Arthroplasty with General Anesthesia Using Propofol or Dexmedetomidine.

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20191104045328N49
Enrollment
146
Registered
2025-12-30
Start date
2026-01-10
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Postoperative Delirium. Delirium due to known physiological condition

Interventions

Intervention 1: Dexmedetomidine group: Patients in this group will receive dexmedetomidine (0.1 µg/kg/h) as a continuous infusion from the time of anesthesia induction until admission to the recovery

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who are candidates for knee arthroplasty under general anesthesia Having informed consent to participate in the study Surgical duration between 60 and 150 minutes

Exclusion criteria

Exclusion criteria: Presence of systemic diseases and history of specific conditions, including renal, hepatic, and cardiovascular diseases, hypertension, diabetes, hematological and vascular diseases, psychotic and mental disorders, Parkinson’s disease, motion sickness, a history of chemotherapy, and malignancies. History of substance use and drug allergies, including absence of opioid use, chronic use of analgesics, hypersensitivity to the medications under study, and seasonal allergies.

Design outcomes

Primary

MeasureTime frame
Occurrence of delirium. Timepoint: After surgery. Method of measurement: Confusion Assessment Method.;Duration of delirium. Timepoint: After surgery. Method of measurement: By the Watch.;Time of onset of delirium. Timepoint: The first, second, and third days after surgery. Method of measurement: Patient file.;Duration until discharge from the recovery unit. Timepoint: After surgical recovery. Method of measurement: Modified Aldrete Score.

Secondary

MeasureTime frame
Mean arterial pressure. Timepoint: At the beginning of surgery and every 15 minutes during the operation, throughout the recovery period, and at 2, 4, and 6 hours after surgery. Method of measurement: NIBP monitoring device.;Heart rate. Timepoint: At the beginning of surgery and every 15 minutes during the operation, throughout the recovery period, and at 2, 4, and 6 hours after surgery. Method of measurement: Cardiac monitoring device.;Arterial blood oxygen saturation. Timepoint: At the beginning of surgery and every 15 minutes during the operation, throughout the recovery period, and at 2, 4, and 6 hours after surgery. Method of measurement: Pulse oximetry.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Alireza Susanabadi

Arak University of Medical Sciences

dr.susanabadi@arakmu.ac.ir+98 86 3222 2003

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026