Effect of SGLT2 Inhibitors on Anemic CKD Patients
Effect of SGLT2 Inhibitors On Anemia in Patients With Chronic Kidney Disease (CKD)
1 other identifier
observational
60
1 country
1
Brief Summary
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
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Jan 2026
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 31, 2025
CompletedStudy Start
First participant enrolled
January 1, 2026
CompletedFirst Posted
Study publicly available on registry
January 12, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
January 14, 2026
January 1, 2026
6 months
December 31, 2025
January 13, 2026
Conditions
Outcome Measures
Primary Outcomes (2)
hemoglobin level
use the hemoglobin level to assist the effect of SGLT2 inhibitors On anemia correction
12 weeks
change in hemoglobin level
anemia correction
12 weeks
Study Arms (1)
CKD patients stage 1_4
Interventions
prescription of SGLT2 inhibitors like dapagliflozin or empagliflozin to anemic CKD patients stage 1\_4
Eligibility Criteria
people in sohag twen
You may qualify if:
- 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
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sohag Universitylead
Study Sites (1)
Sohag University Hospital
Sohag, Sohag University, Egypt
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Romany Naguib Mikhaeil, master
Sohag University
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- resident of internal medicine at sohag university hospital
Study Record Dates
First Submitted
December 31, 2025
First Posted
January 12, 2026
Study Start
January 1, 2026
Primary Completion (Estimated)
July 1, 2026
Study Completion (Estimated)
September 1, 2026
Last Updated
January 14, 2026
Record last verified: 2026-01