High Neutrophil-to-Lymphocyte Ratio and Patients With Hemodialysis

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSohag University

About this trial

To explore the role of neutrophil-to-lymphocyte ratio ( NLR ) and platelet-to-lymphocyte ratio ( PLR ) in predicting mortality in hemodialysis (HD) patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

• Patients aged < 18 years old.

Patient with autoimmune disease.

Patient with liver cirrhosis.

Patients with immunodeficiency.

Trial population

patients on regular hemodialysis

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • neutrophil lymphocyte ratio and platelet lymphocyte ratio

    Other intervention

    explore the role of neutrophil-to-lymphocyte ratio ( NLR ) and platelet-to-lymphocyte ratio ( PLR ) in predicting mortality in hemodialysis (HD) patients

Treatment groups

No treatment groups listed

Trial outcomes

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.

Time frame
6 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: