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Not yet recruiting NCT07354958

Impact of Diabetes-Related Metabolic Derangements on Clinical Outcomes in Hospitalized Patients With Chronic Kidney Disease

Observational Diabetic Chronic Kidney Disease Patients

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Primary aim 1. To assess the frequency of diabetes mellitus among hospitalized CKD patients. 2. To evaluate the frequency and types of metabolic abnormalities (e.g., hypoglycemia, diabetic ketoacidosi.
Who it may be relevant to
Registry conditions: Diabetic Chronic Kidney Disease Patients. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Egypt
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

This observational study will collect clinical and laboratory information from hospitalized patients with chronic kidney disease to identify diabetes mellitus and selected metabolic findings during hospitalization

Detailed description

Hospitalized adult patients with chronic kidney disease will be included in this observational study. Information routinely recorded during hospitalization will be collected. This information will include the presence of diabetes mellitus and laboratory values related to blood glucose levels, electrolyte levels, and acid base balance. No study related interventions will be performed.

Interventions

  • Behavioral Primary aim 1. To assess the frequency of diabetes mellitus among hospitalized CKD patients. 2. To evaluate the frequency and types of metabolic abnormalities (e.g., hypoglycemia, diabetic ketoacidosi
    Primary aim 1. To assess the frequency of diabetes mellitus among hospitalized CKD patients. 2. To evaluate the frequency and types of metabolic abnormalities (e.g., hypoglycemia, diabetic ketoacidosis/ hyperosmolar states, metabolic acidosis, dyslipidemia, electrolyte imbalance) in diabetic CKD patients. Secondary aim 1\. To evaluate the association between diabetes and diabetes-related metabolic derangements in-hospital adverse outcomes (major cardiovascular events, ICU admission, length of

Primary outcome measures

  • In-Hospital Mortality [Time frame: From admission until hospital discharge, assessed over a 6-month study enrollment period.]
  • New Requirement for In-Hospital Renal Replacement Therapy [Time frame: From admission until hospital discharge, assessed over a 6-month study enrollment period.]
  • Incidence of a Major In-Hospital Cardiovascular Composite Event [Time frame: From admission until hospital discharge, assessed over a 6-month study enrollment period.]

Eligibility criteria

Inclusion criteria

  • Age greater than or equal to 18 years
  • Known chronic kidney disease, defined as baseline estimated glomerular filtration rate less than 60 milliliters per minute per 1.73 square meters for at least 3 months, or documented chronic kidney disease stage 3 to 5 by prior medical records
  • Hospitalized for any medical reason
  • Consent provided

Exclusion criteria

  • Acute single episode of reversible acute kidney injury with previously normal renal function (no established chronic kidney disease)
  • Admission for palliative care or expected survival less than 24 hours
  • Pregnancy

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Egypt · 1 center
  • Sohag University Hospital — Sohag

Identifiers

NCT: NCT07354958 · Soh-Med--25-12-5MS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗