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Intravenous Anesthesıa and Cognıtıve Functıon ın Spınal Surgery

The Effect of Two Dıfferent Intravenous Anesthesıa Technıques on Cognıtıve Functıons ın Spınal Surgery

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07701187
Enrollment
128
Registered
2026-07-14
Start date
2023-09-22
Completion date
2024-09-22
Last updated
2026-07-14

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

Conditions

Postoperative Cognitive Dysfunction (POCD)

Keywords

target-controlled infusion, Manuel-controlled infüsion, propofol, Post-Operative Cognitive Dysfunction

Brief summary

The aim of this study is to investigate the effect of these two different intravenous infusion techniques \[manuel controlled infusion (MCI) and Target controlled Infusion( TCI)\] on POCD. To assess POCD, the Mini Mental State Examination (MMSE ) and the Montreal Cognitive Assessment (MoCA ) will be used. MoCA and MMSE have high sensitivity and specificity for identifying patients with mild cognitive impairment who perform within the normal range. In a study by Meng et al., comparing target-controlled infusion and manual infusion of propofol anesthesia during electroconvulsive therapy, the randomized, controlled trial showed no significant difference in postelectroconvulsive therapy changes in MoCA scores in either group; however, they reported improvement in MoCA scores after 6 electroconvulsive therapy treatments in the MCI group, while deterioration occurred in the TCI group. Researchers found no studies investigating the effects of both infusion methods in spinal surgery and their impact on cognitive function, and they planned to evaluate the effects of the groups in their study.

Interventions

DEVICEManuel controlled infusion group

infusion via manually controlled infusion pumps

Sponsors

Bursa Yuksek Ihtisas Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Turkish language proficiency, * age (18-65 years), * American Society of Anesthesiologists (ASA) I-III score, * elective spinal surgery.

Exclusion criteria

* \- refusal to participate * central nervous system disorders, * use of antidepressants or antipsychotic medications, * alcohol or drug use, * illiteracy.

Design outcomes

Primary

MeasureTime frameDescription
Post-Operative Cognitive Dysfunctionpreoperatively and 24 hours postoperatively at the patient's bedsideMontreal Cognitive Assessment (MoCA) scores Normally accepted threshold values: A score of 26 or higher on the MoCA (Montreal Cognitive Assessment) test For cognitive impairment: A decrease of at least 1-2 points on the MoCA is considered significant.

Secondary

MeasureTime frameDescription
Evaluation of intraoperative anaesthezic consumptionintraoperatıvetotal propofol and total remifentanil

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 15, 2026