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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01801345
Other study ID # EH12-048
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 2012
Est. completion date April 2015

Study information

Verified date September 2019
Source NorthShore University HealthSystem
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The primary aim of this randomized controlled trial is to examine the effect of fatigue on clinical performance in a simulated obstetric emergency. This scenario was chosen because it is a common clinical situation faced by anesthesia providers on call and therefore likely to occur when a provider is fatigued. Secondary outcomes will include the evaluation of other factors that worsen fatigue related decrement in performance including age, years of training/practice and clinical load prior to study participation.


Recruitment information / eligibility

Status Completed
Enrollment 13
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- All attending anesthesiologists taking overnight call at Evanston Hospital will be eligible participants.

Exclusion Criteria:

- Resident physician or trainee, physician not taking overnight in house call.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Fatigued

Rested


Locations

Country Name City State
United States Evanston Hospital Evanston Illinois

Sponsors (1)

Lead Sponsor Collaborator
NorthShore University HealthSystem

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Clinical performance Score Performance score on Stat c-section rating scale based on video rating by 2 raters 24 months
Secondary Stanford Sleepiness Scale SSS scores in rested and fatigue arms 24months
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