The Effect of the Severity of COVID-19 Disease on the Incidence of Acute Renal Failure in ICU

Sponsor
Ankara City Hospital Bilkent (Other)
Overall Status
Completed
CT.gov ID
NCT04799600
Collaborator
(none)
158
1
10
15.9

Study Details

Study Description

Brief Summary

Aim of the study is to determinate the frequency of acute renal failure in COVID-19 patients, its relationship with the severity of COVID-19 disease in ICU, and the ability to take precautions against these factors.

Condition or Disease Intervention/Treatment Phase
  • Other: BRESCİA-COVİD Respiratory Severity Scale

Study Design

Study Type:
Observational
Actual Enrollment :
158 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
The Effect of the Severity of COVID-19 Disease on the Incidence of Acute Renal Failure in ICU
Actual Study Start Date :
Sep 1, 2020
Actual Primary Completion Date :
Jun 15, 2021
Actual Study Completion Date :
Jul 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Acute Renal Failure in ICU

COVID-19 Patients with Acute Renal Failure in ICU

Other: BRESCİA-COVİD Respiratory Severity Scale
KDIGO acute renal failure score BRESCİA-COVID Respiratory Severity Score

Outcome Measures

Primary Outcome Measures

  1. KDIGO criteria [6 months]

    KDIGO Criteria stage 1: Increase in SCr by ≥ 0.3 mg/dL within 48 hours or increase in SCr 1.5 to 1.9 times baseline which is known or presumed to have occurred within the prior 7 days Stage 2: 2.0 to 2.9 multiplied by baseline SCr; Stage 3: 3.0 or more multiplied by baseline; increase in SCr ≥ 4.0 mg/dL; or beginning of renal replacement therapy regardless of a previous KDIGO stage.

  2. BRESCIA-COVID RESPIRATORY SEVERITY SCALE (BCRSS) scores [6 months]

    The BCRSS score (between level 0-8) is calculated from "www.mdcalc.com/brescia-covid-respiratory-severity-scale-bcrss-algorithm" according to the severity of COVID disease , respiratory rate, PaO2 level, chest x-ray, and clinical status.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

Patients hospitalized in the intensive care unit diagnosed with COVID-19 will include in the study.

Exclusion Criteria:

there is no exclusion criteria

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ankara City Hospital Ankara Turkey 06800

Sponsors and Collaborators

  • Ankara City Hospital Bilkent

Investigators

  • Principal Investigator: betül aytaç, MD, ankara ch bilkent

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
ismail aytaç, medical doctor, Ankara City Hospital Bilkent
ClinicalTrials.gov Identifier:
NCT04799600
Other Study ID Numbers:
  • E1-20-1443
First Posted:
Mar 16, 2021
Last Update Posted:
Jul 27, 2021
Last Verified:
Jul 1, 2021
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by ismail aytaç, medical doctor, Ankara City Hospital Bilkent
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 27, 2021