Extracellular Water in Covid 19 Pneumonia

Sponsor
Gaziosmanpasa Research and Education Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT04416009
Collaborator
(none)
52
1
7.6
6.9

Study Details

Study Description

Brief Summary

According to various studies Covid 19 pneumonia has a very similar clinical course to Acute Respiratory Distress Syndrome (ARDS) which has clarified by Berlin definition. Based on this similarity, extracellular fluid of lungs and diffuse alveolar damage should be observed in covid 19 pneumonia as well. Extracellular water (ECW) can be determine by using whole body bioimpedence system (NİCaS). The aim of this study is to investigate the effect of ECW on the clinical apperence of covid 19 pneumonia clinical course.

Condition or Disease Intervention/Treatment Phase
  • Device: NİCaS

Detailed Description

Increase in the extracellular water of lungs is the major pathophisilogy of ARDS. According to various studies Covid 19 pneumonia has a very similar clinical course to Acute Respiratory Distress Syndrome (ARDS) which has clarified by Berlin definition. Depending on the similarity of Covid 19 and ARDS; evaluation of ECW ,can be a determinant of clinical apperence of covid19 pneumonia. The aim of this study to find the corelation between ECW and severty of the pneumonia.

In this prospective -controlled research, the patients who were diagnosed with Covid-19 pneumonia will be evaluated. The ones in the intensive care will be considered as severe, and the ones in the ward will be considered as mild clinical course pneumonia. İn both groups, in addition to other heamodynamic parametres, ECW will be recorded using non-invasive body biooimpedence method by NİCaS machine. The total amount of patients will be 52, 26 each two groups.

The ward and intensive care patients will be connected to the NİCaS machine to determine ECW and statistically significantchanges will be recorded. The device consists of a laptop, a software which calculates cardiac parameters and two electrodes. The measurement is done by the following process: one of these electrodes, which looks like ECG electrodes, is stuck to the wrist and the other one to the opposite ankle or each one to two wrists.

the severety of illness will try to be detected.Gpower 3 for Mac Os (Faul, F., Erdfelder, E., Buchner, A., & Lang, A.-G. (2009). Statistical power analyses using G*Power 3.1: Tests for correlation and regression analyses. Behavior Research Methods, 41, 11491160.) was used for istatistical power analysis.The power analysis was done priorly and based on the T-test.In order to provide enoughsample magnitude power, which is 0.8, it was calculated that each group should have 26 patients which makes at total of 52 Statistical method: The normal distribution of data will be evaluated using Kolmogorov-Smirnov test. Parametric ones will be used in normal distrubitions, non-parametric ones will be used in abnormal distrubitions. İntergroup ECW values will be compared via independent sample T test. In catagoric data, the comparisons will be made with Pearson Ki square test, and the p values less then 0.05 will be considered as significant.

Study Design

Study Type:
Observational [Patient Registry]
Anticipated Enrollment :
52 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
the Determination of Extracellular Water (ECW) Which is Detected by Bioimpedence Method on Severe and Mild Covid 19 Pneumonia Clinical Course
Anticipated Study Start Date :
Jul 5, 2020
Anticipated Primary Completion Date :
Dec 20, 2020
Anticipated Study Completion Date :
Feb 20, 2021

Arms and Interventions

Arm Intervention/Treatment
mild pneumonia ECW

the covid 19 pneumonia patients who hospitalised to the ward

Device: NİCaS
whole body bioimpedence method

severe pneumonia ECW

the covid 19 pneumonia patients who hospitalised to the intensive care unit

Device: NİCaS
whole body bioimpedence method

Outcome Measures

Primary Outcome Measures

  1. ECW [three measurements with half an hour intervals]

    Changes of three measurements of extracellular water in both lungs

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:

Covid 19 pneumonia, hospitalized patients older than 18

Exclusion Criteria:

younger than 18 years old, patients not infected with covid 19

Contacts and Locations

Locations

Site City State Country Postal Code
1 Gaziosmanpaşa TREH Istanbul Gaziosmanpaşa Turkey 34255

Sponsors and Collaborators

  • Gaziosmanpasa Research and Education Hospital

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
SİBEL BEKTAŞ, director, Gaziosmanpasa Research and Education Hospital
ClinicalTrials.gov Identifier:
NCT04416009
Other Study ID Numbers:
  • 76
First Posted:
Jun 4, 2020
Last Update Posted:
Jun 4, 2020
Last Verified:
Jun 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
Yes
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by SİBEL BEKTAŞ, director, Gaziosmanpasa Research and Education Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 4, 2020