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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03317106
Other study ID # 2017-07-058
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 8, 2017
Est. completion date August 31, 2018

Study information

Verified date July 2021
Source Chungnam National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

this study examines the incidence of newly developed delirium in patients who admit to university hospital stroke unit for cerebral infarction, and analyze the association between delirium motor subtypes and short-term outcome in post-stroke delirium patients.


Recruitment information / eligibility

Status Completed
Enrollment 943
Est. completion date August 31, 2018
Est. primary completion date March 31, 2018
Accepts healthy volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - All cerebral infarction patients who admit to stroke unit Chungnam National University Hospital. Exclusion Criteria: - Any patients who refuse to enroll the study. - Any patients who admit to Intensive Care Unit(ICU), because ICU is well-known for precipitating delirium.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Korea, Republic of Chungnam National University Hospital Daejeon Munhwa-ro 282, Jung-gu

Sponsors (1)

Lead Sponsor Collaborator
Chungnam National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary mean K-DRS-R98 score mean score of delirium severity rating scale during follow up period. Detailed information about scale: Korean Version of the Delirium Rating Scale-Revised-98(K-DRS-R98) DRS-R98 proved to be a valid and reliable instrument for the assessment of delirium severity and distinguish patients with delirium from non-delirious patients including dementia. The scale is composed of two sections. The first section is the severity scale, which consists of 13 items that are scored from 0 to 3 according to a Likert scale that is anchored by descriptions of phe-nomenology. The second section consists of three diagnostic items that are scored from 0 to 2 or 3. These items include temporal onset of symptoms, fluctuation of symptom severity and physical disorder. The total scale is comprised of 16 items. The total score is the sum of the scores for each item and the higher the score, the greater the severity. 3 weeks
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