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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04434079
Other study ID # 2018-0486
Secondary ID
Status Completed
Phase
First received
Last updated
Start date June 1, 2018
Est. completion date December 1, 2018

Study information

Verified date June 2020
Source Hospital de Clinicas de Porto Alegre
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Positive fluid status has been consistently associated with worse prognosis in critically ill adult patients.However, observational studies showed poor agreement between fluid balance and body weight changes. The objective of the study is to compare the measurements of FB and BW over time and to assess correlation with ICU mortality.


Description:

Positive fluid status has been consistently associated with worse prognosis in critically ill adult patients. Daily and cumulative fluid balance (FB) is a routine nursing activity in intensive care unit (ICU). In view of the potential for errors in the calculation of FB totals and the problem of accounting for insensible fluid losses, measurement of body weight (BW) changes is an alternative non-invasive method commonly used for estimating body fluid status. Its accuracy over FB assumes a one kilogram change in BW equates to a one liter gain or loss in body fluid volume. However, observational studies showed poor agreement between those measurements, particularly among individuals staying more than a week in ICU possibly due to muscle and fat loss as well as bone demineralization. The objective of the study is to compare the measurements of FB and BW over time and to assess correlation with ICU mortality.


Recruitment information / eligibility

Status Completed
Enrollment 98
Est. completion date December 1, 2018
Est. primary completion date October 1, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Individuals aged >18 years-old admitted to ICU;

- Expected length of ICU stay superior to 24 hours.

Exclusion Criteria:

- Individuals receiving oral diet;

- Actual body weight superior to 227kgs or 501lb.

Study Design


Intervention

Other:
Regular critical care
Clinical demographic data, daily and cumulative FB (input minus output) with and without insensible fluid losses, and daily and total BW changes are recorded, as well as survival outcome.

Locations

Country Name City State
Brazil Hospital de Clínicas de Porto Alegre Porto Alegre RS

Sponsors (1)

Lead Sponsor Collaborator
Hospital de Clinicas de Porto Alegre

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Correlation between daily fluid balance (difference between fluid input and output during 24 hours) and the change on daily weight Correlation between daily fluid balance and weight change (Bland-Altman agreement test) At midnight every 24 hours up to patient's ICU discharge or up to 6 months, whichever comes first.
Secondary Correlation between cumulative fluid balance and total weight change Correlation between cumulative fluid balance and total weight change (Bland-Altman) Last day of each patient's ICU hospitalization, up to 6 months
Secondary Discriminative power of fluid balance in predicting ICU mortality Area under ROC curve for fluid balance (L). ICU mortality as reference variable. Through study completion, up to 6 months
Secondary Discriminative power of body weight changes in predicting ICU mortality Area under ROC curve for body weight change (kg). ICU mortality as reference variable. Through study completion, up to 6 months
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