Electrolyte Imbalance Analysis at Intensive Care Unit Admission : Retrospective Study

September 22, 2021 updated by: ESRA OZAYAR, Kecioren Education and Training Hospital

Electrolyte Imbalance Analysis at Icu Admission : Retrospective Study

The type and severity of electrolyte imbalance in patients admitted to the intensive care unit were analyzed.It was evaluated whether these results had an effect on mortality, length of hospital stay, APACHE II scores and ventilator days

Study Overview

Status

Completed

Study Type

Observational

Enrollment (Actual)

824

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Çankaya
      • Ankara, Çankaya, Turkey
        • Ankara Kecioren Training and Research Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

ıcu patients

Description

Inclusion Criteria: all of the ıcu patients -

Exclusion Criteria:

-

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Cohort
  • Time Perspectives: Retrospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
sodium (hypo-hyper-normonatremia)
ın this retrospective study we aimed to evaluate the relationship between the ıcu prognosis and the electrolyte imbalance
potassium (hypo-hyper-normokalemia)
ın this retrospective study we aimed to evaluate the relationship between the ıcu prognosis and the electrolyte imbalance
calcium (hyper-hypo-normocalcemia)
ın this retrospective study we aimed to evaluate the relationship between the ıcu prognosis and the electrolyte imbalance
magnesium (hyper-hypo-normocalcemia)
ın this retrospective study we aimed to evaluate the relationship between the ıcu prognosis and the electrolyte imbalance
phosphor (hypo-hyper-normophosphatemia)
ın this retrospective study we aimed to evaluate the relationship between the ıcu prognosis and the electrolyte imbalance

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The analysis the electrolyte imbalance in ICU and the relationship between the icu prognosis.
Time Frame: 2 years

Natremia (Hypo: <136 mmol/L, Normo: 136-145 mmol/L, Hyper: >145 mmol/L) Kalemia (Hypo: <3.5 mmol/L, Normo: 3.5-5.5 mmol/L, Hyper: >5.5 mmol/L) Calcemia (Hypo: <8.8 mg/dL, Normo: 8.8-10.6 mg/dL, Hyper: >10.6 mg/dL) Magnesemia (Hypo: <1.9 mg/dL, Normo: 1.9-2.5 mg/dL, Hyper: >2.5 mg/dL) Phosphatemia (Hypo: <2.5 mg/dL, Normo: 2.5-4.5 mg/dL, Hyper: >4.5 mg/dL)

The number of patients in all types of electrolyte imbalance will be determined. The effect of the type of electrolyte imbalance on mortality, APACHE-II score and length of invasive ventilation and hospital stay will be evaluated.

2 years

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 10, 2019

Primary Completion (Actual)

April 5, 2021

Study Completion (Actual)

August 15, 2021

Study Registration Dates

First Submitted

September 2, 2021

First Submitted That Met QC Criteria

September 19, 2021

First Posted (Actual)

September 22, 2021

Study Record Updates

Last Update Posted (Actual)

September 28, 2021

Last Update Submitted That Met QC Criteria

September 22, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • erbil elektrolit

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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