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NCT04041947 Clinical Trial

Delirium Assessment in the Pediatric Intensive Care Unit

Delirium Clinical Trial

Official title:
Assessment of Delirium Frequency and Risk Factors in Pediatric Intensive Care Unit

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT04041947
Other study ID # CUTF-GOKAEK-82
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 1, 2018
Est. completion date December 1, 2019

Study information
Verified date February 2020
Source Cukurova University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study was to show the efficacy of non-pharmacological interventions on preventing pediatric delirium in pediatric intensive care unit

Description:

The aim of this study was to show the efficacy of non-pharmacological interventions on preventing pediatric delirium in pediatric intensive care unit. Patients who is followed up for at least 48 hours in pediatric intensive care unit will be included in the study. Parents of patients will be allowed to stay with the patient as long as the conditions of service is appropriate. Parents will provide oral treatments to the patients. Patients will be allowed to spend time with their phone, tablet or toy in accordance with their age. Fellow resident will screen for pediatric delirium each child using the Cornell Assessment of Pediatric Delirium twice a day.

Recruitment information / eligibility
Status Completed
Enrollment 140
Est. completion date December 1, 2019
Est. primary completion date September 1, 2019
Accepts healthy volunteers No
Gender All
Age group 1 Month to 18 Years
Eligibility Inclusion Criteria:

- Pediatric Cerebral Performance Category < 5 points

- Patients who stay in PICU >48 hours

Exclusion Criteria:

- Pediatric Cerebral Performance Category > 4 points

- Patients who stay in PICU <48 hours

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Turkey Cukurova University Medicine Faculty Adana

Sponsors (1)
Lead Sponsor Collaborator
Cukurova University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pediatric delirium frequency The effect of non-pharmacological interventions on the prevalence of pediatric delirium Up to a month
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