NCT07179211

Brief Summary

Recent studies have reinforced the association between high NLR and PAD in hemodialysis patients. This highlights the need for further studies to confirm its predictive value and determine optimal cut-off thresholds tailored to local patient populations. Accordingly, the present study aims to investigate the relationship between NLR and the presence of PAD in patients undergoing regular hemodialysis. By establishing this association in a well-defined population, we hope to provide evidence that supports the use of NLR as a simple, cost-effective tool for PAD risk stratification and early intervention

Trial Health

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for all trials

Timeline
2mo left

Started Jul 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress82%
Jul 2025Jul 2026

Study Start

First participant enrolled

July 13, 2025

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

September 2, 2025

Completed
15 days until next milestone

First Posted

Study publicly available on registry

September 17, 2025

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 13, 2026

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 13, 2026

Expected
Last Updated

September 17, 2025

Status Verified

September 1, 2025

Enrollment Period

6 months

First QC Date

September 2, 2025

Last Update Submit

September 10, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • The aim of this study is to evaluate the predictive value of the neutrophil-to- lymphocyte ratio (NLR) for the presence of peripheral artery disease (PAD) in patients undergoing regular hemodialysis.

    6months

  • % of patients with affection in neutrophills to lymphocytes ratio in parient on regular hemodialysis.

    6 months

Eligibility Criteria

Sexall
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

The present study aims to investigate the relationship between NLR and the presence of PAD in patients undergoing regular hemodialysis. By establishing this association in a well-defined population, we hope to provide evidence that supports the use of NLR as a simple, cost-effective tool for PAD risk stratification and early intervention

You may qualify if:

  • Adult patients aged ≥18 years.
  • Undergoing maintenance hemodialysis for at least 3 months (thrice weekly)
  • Able to provide informed consent.
  • Willing to undergo clinical and laboratory evaluations, including peripheral vascular assesment

You may not qualify if:

  • Active infection or sepsis at the time of evaluation
  • \* Patients who have a sedimentation rate of more than 60 mm/hour
  • \*. Known autoimmune or hematologic disorders that may influence leukocyte count.
  • Current use of immunosuppressive therapy, corticosteroids, or chemotherapy.5. History of malignancy.6. Patients with incomplete medical records or unable to undergo peripheral vascular assessment.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Sohag faculty

Sohag, Egypt

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

CBC CRP Lipid profile

MeSH Terms

Conditions

Renal Insufficiency, Chronic

Condition Hierarchy (Ancestors)

Renal InsufficiencyKidney DiseasesUrologic DiseasesFemale Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsUrogenital DiseasesMale Urogenital DiseasesChronic DiseaseDisease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Target Duration
120 Months
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Resident physician in the Department of General Internal Medicine

Study Record Dates

First Submitted

September 2, 2025

First Posted

September 17, 2025

Study Start

July 13, 2025

Primary Completion

January 13, 2026

Study Completion (Estimated)

July 13, 2026

Last Updated

September 17, 2025

Record last verified: 2025-09

Locations