NCT07380893

Brief Summary

The goal of this observational study is to determine the prevalence of left ventricular hypertrophy among patients with chronic kidney disease at Sohag University Hospital and assess the effect of erythropoietin therapy on left ventricular mass and geometry in anemic CKD patients. The main question it aims to answer is: Does erythropoietin therapy mitigate or even reverse LVH and improve cardiac geometry ?

Trial Health

65
Monitor

Trial Health Score

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

Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
2mo left

Started Jan 2026

Shorter than P25 for all trials

Status
not yet recruiting

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

Study Progress62%
Jan 2026Jul 2026

First Submitted

Initial submission to the registry

December 30, 2025

Completed
16 days until next milestone

Study Start

First participant enrolled

January 15, 2026

Completed
18 days until next milestone

First Posted

Study publicly available on registry

February 2, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 15, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

July 15, 2026

Last Updated

February 2, 2026

Status Verified

January 1, 2026

Enrollment Period

5 months

First QC Date

December 30, 2025

Last Update Submit

January 24, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Change in LVMI following erythropoietin therapy in anemic CKD patients.

    - baseline transthoracic echocardiography will be performed for all group study.

Secondary Outcomes (1)

  • Association between hemoglobin level and LVMI.

    6 months of erythropoitin therapy , transthoracic echocardiography will be performed for all group study.

Interventions

Standard transthoracic echocardiography will be performed for all participants, measuring: * Left ventricular end-diastolic diameter (LVEDD) * Interventricular septal thickness (IVSD) * Posterior wall thickness (PWD) * Left ventricular mass (LVM) * Left ventricular mass index (LVMI = LVM/body surface area)

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

study population is adults age (18-75)years, diagnosed with CKD stage 3-5 .

You may qualify if:

  • Adults (≥18 years) diagnosed with CKD stages 3-5.
  • Stable clinical condition for ≥3 months.
  • Anemia (Hb \<10 g/dL) for cohort phase.
  • Willingness to participate and provide informed consent.

You may not qualify if:

  • Valvular or ischemic heart disease.
  • Uncontrolled hypertension (BP \>180/110 mmHg).
  • Acute coronary syndrome or decompensated heart failure in the past 3 months.
  • Malignancy or active infection

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Hypertrophy, Left Ventricular

Condition Hierarchy (Ancestors)

CardiomegalyHeart DiseasesCardiovascular DiseasesHypertrophyPathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Study Officials

  • Amal Kh Ahmed, MD

    Sohag university- faculty of medicine - internal medicine department

    STUDY CHAIR

Central Study Contacts

khaled M Mohamedein, MBCHB

CONTACT

Marwa Z Elsayed, MD

CONTACT

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
resident of internal medicine

Study Record Dates

First Submitted

December 30, 2025

First Posted

February 2, 2026

Study Start

January 15, 2026

Primary Completion (Estimated)

June 15, 2026

Study Completion (Estimated)

July 15, 2026

Last Updated

February 2, 2026

Record last verified: 2026-01