Sedation and Postoperative Cognitive Functions

NCT ID: NCT05737459

Last Updated: 2023-02-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

82 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-05-01

Study Completion Date

2022-12-31

Brief Summary

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Patients over the age of 65 who underwent elective surgery for a hip fracture and were sedated during spinal anesthesia were included in the study. Patients who were given ketamine and dexmedetomidine for sedation were included in the study. The Mini Mental Status Tests of the patients measured on the first and third days of the operation in the preoperative period were determined from the hospital records and recorded.

Detailed Description

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Patients over the age of 65 who underwent elective surgery for a hip fracture and were sedated during spinal anesthesia were included in the study. The cognitive functions of these patients, which were evaluated by a Mini-Mental Test in the preoperative period, on the first and third days of surgery, were recorded from routine patient follow-up forms.

Sedation scores of the patients evaluated by Intraoperative Alertness/Sedation Scale (OAA/S) Observer Evaluation were recorded. Intraoperative hemodynamic data were recorded. The interventions applied to the patient were performed by anesthesiologists who were not involved in the study according to their preferences as part of the routine. The researchers were not involved in any intervention performed on the patient, only the data were recorded.

Conditions

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Cognitive Impairment Femoral Fractures

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Group K

Those who have been administered ketamine for perioperative sedation

No interventions assigned to this group

Group D

Those who have been administered dexmedetomidine for perioperative sedation.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Patients over the age of 65 who underwent surgery under spinal anesthesia due to hip fracture
* Volunteered to participate in the study

Exclusion Criteria

* Patients who are under the age of 65
* Patients with known histories of dementia
* Patients with Alzheimer's disease
* Patients with central nervous system disease
* Patients who scored 15 or less according to the Mini Mental Status Test (MMSE)
* Patients who underwent surgery under general anesthesia
* Patients who refused to voluntarily participate in the study
Minimum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Izmir Ataturk Training and Research Hospital

OTHER

Sponsor Role lead

Responsible Party

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Derya Arslan Yurtlu

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Derya A Yurtlu, M.D.

Role: PRINCIPAL_INVESTIGATOR

Izmir Katip Celebi University Atatürk Training and Research Hospital

Locations

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Izmir Katip Çelebi University Atatürk Training and Research Hospital

Izmir, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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IAERH

Identifier Type: -

Identifier Source: org_study_id

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