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Role of intra-operative cerebral oximetry with post-operative cognitive dysfunction

Correlation of intra-operative cerebral oximetry with incidence of post-operative cognitive dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2019/06/019779
Enrollment
61
Registered
2019-06-20
Start date
Unknown
Completion date
Unknown
Last updated
2023-04-03

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

Conditions

Health Condition 1: D334- Benign neoplasm of spinal cord Health Condition 2: D321- Benign neoplasm of spinal meninges Health Condition 3: M500- Cervical disc disorder with myelopathy Health Condition 4: M509- Cervical disc disorder, unspecified Health Condition 5: Q079- Congenital malformation of nervoussystem, unspecified Health Condition 6: G379- Demyelinating disease of central nervous system, unspecified Health Condition 7: C720- Malignant neoplasm of spinal cord Health Condition 8: M502- Ot

Interventions

Intervention1: na: na

Sponsors

NIMHANS
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: spine surgery in prone position

Exclusion criteria

Exclusion criteria: 1)Spinal surgery in supine position 2)Patients aged less than 18 years, 3)Patients with uncontrolled diabetes mellitus, past history of myocardial infarction, post CABG or stenting and those with significant valvular disease 4)Patients with ASA-Physical Status III, IV

Design outcomes

Primary

MeasureTime frame
To determine the incidence of Post Operative Cognitive Dysfunction 2) To determine the correlation of cerebral oximetry with Post-Operative Cognitive Dysfunction in patients undergoing spinal surgery in prone position. Timepoint: 48hrs after surgery

Secondary

MeasureTime frame
1)Spinal surgery in supine position 2)Patients aged less than 18 years, 3)Patients with uncontrolled diabetes mellitus, past history of myocardial infarction, post CABG or stenting and those with significant valvular disease 4)Patients with ASA-Physical Status III, IV Timepoint: 48hours Post surgery

Countries

India

Contacts

Public ContactDr Nupur Karan

National Institute of Mental Health And Neurosciences

krmsr2000@yahoo.com

Outcome results

None listed

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