- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07070557
- Original Trial
High Neutrophil-to-Lymphocyte Ratio and Patients With Hemodialysis
July 16, 2025 updated by: Bassem Ayman Mohamed, Sohag University
High Neutrophil-to-Lymphocyte Ratio and Platelet-to-Lymphocyte Ratio Are Associated With Poor Survival in Patients With Hemodialysis
To explore the role of neutrophil-to-lymphocyte ratio ( NLR ) and platelet-to-lymphocyte ratio ( PLR ) in predicting mortality in hemodialysis (HD) patients.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
100
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
سوهاج
-
Sohag, سوهاج, Egypt
- Hemodialysis Unit
-
Contact:
- ali taha, professor of internal medicine
- Phone Number: 01005871047
- Email: alitaha23222@gmail.com
-
Contact:
- marwa zanaty, lecture of internal medicine
- Phone Number: 01007100970
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
patients on regular hemodialysis
Description
Inclusion Criteria:
- 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
Exclusion Criteria:
• Patients aged < 18 years old.
- Patient with autoimmune disease.
- Patient with liver cirrhosis.
- Patients with immunodeficiency.
- Patients with malignancy.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Mortality
Time Frame: 6 months
|
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
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Estimated)
July 15, 2025
Primary Completion (Estimated)
February 15, 2026
Study Completion (Estimated)
May 1, 2026
Study Registration Dates
First Submitted
July 6, 2025
First Submitted That Met QC Criteria
July 16, 2025
First Posted (Actual)
July 17, 2025
Study Record Updates
Last Update Posted (Actual)
July 17, 2025
Last Update Submitted That Met QC Criteria
July 16, 2025
Last Verified
July 1, 2025
More Information
Terms related to this study
Other Study ID Numbers
- Soh-Med--25-6-10MS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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