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The effect of anesthesia types on cognitive disorders after spinal surgery

Evaluation of postoperative cognitive disorders in non-emergent spinal surgery patients undergoing intravenous and isoflurane anesthesia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20211023052849N3
Enrollment
65
Registered
2022-06-08
Start date
2022-02-24
Completion date
Unknown
Last updated
2022-06-27

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

Conditions

Spine surgery. Injury of nerve root of thoracic spine, subsequent encounter

Interventions

Intervention 1: Group 1 will be patients who are candidates for elective spinal surgery and will receive anesthesia with complete intravenous drugs by propofol induction dose(2-2.5 mg/kg IV) .After in

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: = 18 years of age and maximum 65 Class 1 to 3 ASA anesthesia Absence of heart failure (EF <20%) No uncontrolled blood pressure or diabetes No pregnancy Willingness and satisfaction to participate in the project

Exclusion criteria

Exclusion criteria: Emergent surgery Patient dissatisfaction with continued participation in the study Pregnant women History of using psychiatric medications History of dementia History of brain surgery History of schizophrenia Recent alcohol or opioid use Severe anxiety Mental retardation Recent stroke

Design outcomes

Primary

MeasureTime frame
Cognitive disorders. Timepoint: Before induction of anesthesia, 6 ,12 , and 24 hours after Recovery. Method of measurement: Mini Mental State Examination questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactArash Heroabadi

Tehran University of Medical Sciences

arash.heroabadi@gmail.com+98 21 8490 1000

Outcome results

None listed

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