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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02529696
Other study ID # 1502M62761
Secondary ID
Status Terminated
Phase
First received
Last updated
Start date September 30, 2015
Est. completion date May 31, 2019

Study information

Verified date June 2022
Source University of Minnesota
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Maintenance of analgesia during a patient stay in the hospital has been an important area of investigation after demonstrating a direct correlation between level of sedation and mortality in the ICU setting. This study will investigate the use of accelerometers in determining patient sedation level.


Description:

The goal of the study is to use accelerometers to track patient movement while under sedation in the ICU. Analysis of patient movement may reveal objective means to measuring patient level of sedation. Average length of stay is estimated to be one week.


Recruitment information / eligibility

Status Terminated
Enrollment 60
Est. completion date May 31, 2019
Est. primary completion date May 31, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria: - Admitted to the neuro ICU at University of Minnesota Exclusion Criteria: - Unable to wear accelerometer device

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Accelerometer
Measures patient movement

Locations

Country Name City State
United States University of Minnesota Minneapolis Minnesota

Sponsors (1)

Lead Sponsor Collaborator
University of Minnesota

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Accelerometer movement Movement during stay in the ICU. Duration of ICU stay: estimated to be one week
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