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Clinical Trials/NCT02077816
NCT02077816CompletedNot Applicable

Using Non-contact Infrared Thermometry to Detection of Central Venous Catheter Related Infection.

University of Sao Paulo1 site in 1 country39 target enrollmentStarted: August 2011Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
39
Locations
1
Primary Endpoint
Body temperature measured with a non-contact infrared thermometer.

Study Overview

Brief Summary

This is a pilot study which aims to show the temperatures measured on body surface with an infrared thermometer on inpatients who need a central venous catheter (CVC) for medical care. Because the local temperature could be altered, at least during local infectious processes, seems to be reasonable to think that this approach could be helpful to its early diagnosis.

Detailed Description

By convenience sampling, it was expected that during 4 months, a minimum of 30 inpatients of the metabolic, clinical or intensive care wards, at the Clinical Hospital of Ribeirão Preto Medical School, São Paulo, Brazil, would have their data collected

Study Design

Study Type
Observational
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Need of a central venous catheter for medical care.
  • Be an inpatient of the metabolic, clinical or intensive care wards

Exclusion Criteria

  • Be in treatment course of a catheter related infection.

Outcomes

Primary Outcomes

Body temperature measured with a non-contact infrared thermometer.

Time Frame: 15 minutes after bath, mobilization or warm or cold compresses

It was used a non-contact forehead infrared thermometer, model IR200® (Extech, USA). Fifteen minutes after bath, mobilization or warm or cold compresses, 3 measurements were obtained at the following sites: 1) close to CVC insertion, 2) at the equivalent contralateral site of CVC and 3) at the forehead. The variables values will be displayed in form of descriptive statistics (mean, standard deviation, standard error, proportions of the observations, confidence intervals) according to: sex, central venous catheter type (guide wire or port-a-cath), location of insertion, reason of the central venous catheter indication (like parenteral nutrition or antibiotics), number of catheter lumens and age. Also, the mean differences between the three locations measured will be presented.

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Julio Sergio Marchini

Full Professor of Internal Medicine Department at Ribeirão Preto Medical School

University of Sao Paulo

Study Sites (1)

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