Chronic Kidney Disease, Hyperkalemia and Echocardiographic Changes

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSaglik Bilimleri Universitesi

About this trial

Patients with CKD ( eGFR \< \<60 mL/min/1,73 m2) presenting to emergency department with isolated hyperkalemia will be study population. Pre and post treatment ECG and echocardiographic findings will be recorded. Investigator will not intervene with the treatment decision of responsible physician and will not delay any intervetion or treatment for the sake of study.

Data will be compared in terms of ECHO and ECG findings depending on hyperkalemia level and response to treatment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients over 18 years old

Chronic kidney disease patients with eGFR < 60 mL/min/1.73 m²

Patients with hyperkalemia detected in the emergency department

Patients willing to participate in the study and who sign the consent form

Disqualifiers

Patients under 18 years old

Patients who do not wish to participate in the study

Patients without chronic kidney damage

Patients without detected hyperkalemia

Trial population

Patient with chronic kidney disease presenting to emergency department and having isolated hyperkalemia with or without ECG changes

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

40 Participants
are grouped into 1 trial group
Group A: Hyperkalemia

Trial outcomes

Primary outcomes

1

ECHO changes

Describing echocardiograhic (ECHO) changes of isolated hyperkalemia in patients with chronic kidney disease (CKD)

Time frame
from enrollment to the end of follow up duration of 30 days

Secondary outcomes

Other outcomes

Sponsors and contacts

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