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Application of Serial Body Composition Change for Risk Prediction in Treating Patients With Severe Pneumonia

Application of Serial Body Composition Change for Risk Prediction in Treating Patients With Severe Pneumonia

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04396522
Enrollment
194
Registered
2020-05-20
Start date
2019-05-01
Completion date
2023-02-21
Last updated
2023-09-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pneumonia

Keywords

pneumonia, sepsis, body composition

Brief summary

We hypothesize that serial changes of body composition in patients with pneumonia can help clinician to monitor prognosis. It was associated with underlying immune response.

Detailed description

Specific aims: 1. Can serial body composition data be useful for predicting outcomes of patients with pneumonia? (developing sepsis, organ failure, admission to ICU, length of ICU, survival, length of stay in hospital, prolonged mechanical ventilation,..) 2. Can serial body composition data be integrated into both immune status alternatives (e.g., white blood cell (WBC) count, segment/monocyte ratio, pulse pressure) in such critical illness and monitoring responses (SOFA score, labs) for severe pneumonia patients? 3. Can serial body composition data reflect clinical variables in patients with pneumonia, and even altered by nutrition intake? (e.g., compare association between nutrition intake amount and groups stratified by body composition, blood pressure, nutritional intake, …)

Interventions

DEVICEnoninvasively Bio-electrical Impedance Analysis (BIA)

By means of noninvasively Bio-electrical Impedance Analysis (BIA) to measure body composition, which divides body weight into different components such as lean body mass and fat mass.

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Adult patients with pneumonia admitted to the thoracic ward or medical intensive care unit of Kaohsiung Chang Gung Memorial Hospital

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frameDescription
ICU DaysDuring hospitalization, through study completion, an average of 1 yearlength of stay in ICU
Ventilation daysup to 24 weeksdays of mechanical ventilation
sepsis free daysup to 24 weeksthe cure day of sepsis
mortalityDuring hospitalization, through study completion, an average of 1 yeardeath rate
Change in Total Body WaterChange from Baseline Total Body Water at day 8Change in Total Body Water
Change in Percentage of Body FatChange from Baseline Percentage of Body Fat at day 8Change in Percentage of Body Fat
Change in Soft Lean MassChange from Baseline Soft Lean Mass at day 8Change in Soft Lean Mass
Change in segment/monocyte ratioChange from Baseline Segment count to monocyte count ratio at day 8Change in Segment count to monocyte count ratio

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026