High Neutrophil-to-Lymphocyte Ratio and Patients With Hemodialysis
1 other identifier
observational
100
1 country
1
Brief Summary
To explore the role of neutrophil-to-lymphocyte ratio ( NLR ) and platelet-to-lymphocyte ratio ( PLR ) in predicting mortality in hemodialysis (HD) patients.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jul 2025
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
July 6, 2025
CompletedStudy Start
First participant enrolled
July 15, 2025
CompletedFirst Posted
Study publicly available on registry
July 17, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 15, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 1, 2026
CompletedJuly 17, 2025
July 1, 2025
7 months
July 6, 2025
July 16, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Mortality
The primary outcome measures in the study "High Neutrophil-to-Lymphocyte Ratio and Platelet-to-Lymphocyte Ratio Are Associated with Poor Survival in Patients with Hemodialysis" is :- All-cause mortality, encompassing death from any cause These is the endpoint used to evaluate the prognostic significance of NLR and PLR in hemodialysis patients.
6 months
Interventions
explore the role of neutrophil-to-lymphocyte ratio ( NLR ) and platelet-to-lymphocyte ratio ( PLR ) in predicting mortality in hemodialysis (HD) patients
Eligibility Criteria
patients on regular hemodialysis
You may qualify if:
- All cases with age ≥ 18 years from both sexes female and male, having end-stage renal disease (ESRD), who have been on hemodialysis for at least three months and divided to 4 groups according to the median of NLR and PLR
You may not qualify if:
- Patients aged \< 18 years old.
- Patient with autoimmune disease.
- Patient with liver cirrhosis.
- Patients with immunodeficiency.
- Patients with malignancy.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sohag Universitylead
Study Sites (1)
Hemodialysis Unit
Sohag, Sohag Governorate, Egypt
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- resident in internal medicine department
Study Record Dates
First Submitted
July 6, 2025
First Posted
July 17, 2025
Study Start
July 15, 2025
Primary Completion
February 15, 2026
Study Completion
May 1, 2026
Last Updated
July 17, 2025
Record last verified: 2025-07