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Not yet recruiting NCT07334145

Effect of SGLT2 Inhibitors on Anemic CKD Patients

Observational Anemia in CKD 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: SGLT2 inhibitor.
Who it may be relevant to
Registry conditions: Anemia in CKD 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 →
Official title

Effect of SGLT2 Inhibitors On Anemia in Patients With Chronic Kidney Disease (CKD)

Overview

anemia is a common complication of CKD patients and affect the quality of life and increase morbidity and mortality. managing anemia in CKD patients remains challenging conventional therapy including iron and ESAs which has its complications. the SGLT2 inhibitors have emerging evidence from major clinical trials in improving anemia in patients with CKD

Interventions

  • Drug SGLT2 inhibitor
    prescription of SGLT2 inhibitors like dapagliflozin or empagliflozin to anemic CKD patients stage 1\_4

Primary outcome measures

  • hemoglobin level [Time frame: 12 weeks]
  • change in hemoglobin level [Time frame: 12 weeks]

Eligibility criteria

Inclusion criteria

  • age more than 18 years
  • CKD stage 1\_4
  • baseline hemoglobin 8.5 to 12.9 g/dl
  • stable anemia regimen for more than 8 weeks

Exclusion criteria

  • dialysis recent blood transfusion or ESA dose change within 8 weeks active malignancy or infection pregnancy or lactation history of recurrent DKA or sever volume depletion

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

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Egypt · 1 center
  • Sohag University Hospital — Sohag

Identifiers

NCT: NCT07334145 · soh_med__25_12_6MS

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗