RDW to Platlet Count Ratio in CKD Patients

Sponsor
Sohag University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05754827
Collaborator
(none)
100
12.9

Study Details

Study Description

Brief Summary

The aim of the study is to determine Red blood cell distribution width to platelet count ratio as a predictor of cardiovascular complications in CKD patients

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: RDW to platlet count ratio

Detailed Description

comparative study between RDW to Platlet count ratio in CKD patients without cardiovascular complications and CKD patients with cardiovascular complications

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Red Blood Cell Distribution Width to Platelet Count Ratio as a Predictor of Cardiovascular Complications in CKD Patients
Anticipated Study Start Date :
Feb 22, 2023
Anticipated Primary Completion Date :
Feb 22, 2024
Anticipated Study Completion Date :
Mar 22, 2024

Arms and Interventions

Arm Intervention/Treatment
1-CKD patients without cardiovascular complications

Diagnostic Test: RDW to platlet count ratio
RDW to platlet ratio will be measured for all patients and results will be compared between groups

2-CKD patients with cardiovascular complications

Diagnostic Test: RDW to platlet count ratio
RDW to platlet ratio will be measured for all patients and results will be compared between groups

Outcome Measures

Primary Outcome Measures

  1. Comparison of results of RDW to platlet ratio in CKD patients [1 year]

    Calculate RDW to platlet ratio for CKD patints with or without cardiovascular complications and compare the results

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
  • Inclusion Criteria:

  • CKD Patients and patients receive dialysis >18 years old

  • Exclusion Criteria:

  • Serious complications of any other organs

  • patients who had previously undergone kidney transplantation .

  • CKD patients with history of previous CVD

  • patients with an infection, blood transfusion or receiving immunosuppressive drugs, as this may have affected the inflammatory response within the 3 months

  • patients who were pregnant

  • patients with chronic hematological disease

  • patient<18 years

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Sohag University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Doha Aly Mohamed, Dr, Sohag University
ClinicalTrials.gov Identifier:
NCT05754827
Other Study ID Numbers:
  • CKD and CV complications
First Posted:
Mar 6, 2023
Last Update Posted:
Mar 6, 2023
Last Verified:
Mar 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Mar 6, 2023