Predictors of Rapid CKD Progression

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

About this trial

This prospective observational cohort study aims to identify independent predictors of rapid chronic kidney disease (CKD) progression and determine its incidence among predialysis CKD patients. A total of 190 adult patients will be enrolled from the nephrology outpatient clinic and inpatient ward at Assiut University Hospitals and followed for 24 months. Rapid progression is defined as a sustained decline in eGFR \> 5 mL/min/1.73 m² per year according to KDIGO 2024 criteria. Clinical and laboratory parameters will be assessed at baseline and during follow-up to identify predictive factors

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 18 years or older

Diagnosis of CKD according to KDIGO 2024 criteria

Predialysis status (not on maintenance dialysis)

Ability to provide written informed consent

Disqualifiers

Acute kidney injury

Current maintenance dialysis

Previous kidney transplantation

Active malignancy

Trial population

Adult patients with predialysis chronic kidney disease (CKD) attending the Nephrology outpatient clinic and inpatient ward at Assiut University Hospitals.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

190 Participants
are grouped into 1 trial group
Group A: Predialysis CKD Patients

Trial outcomes

Primary outcomes

1

Incidence of rapid CKD progression

Proportion of participants who experience rapid CKD progression, defined as a sustained decline in eGFR greater than 5 mL/min/1.73 m² per year.

Time frame
24 months

Secondary outcomes

1

Independent predictors of rapid CKD progression

Clinical and laboratory variables independently associated with rapid CKD progression using multivariate logistic regression analysis.

Time frame
24 months
2

Change in estimated glomerular filtration rate (eGFR)

Absolute change in eGFR (mL/min/1.73 m²) from baseline to follow-up visits.

Time frame
Baseline, 12 months, and 24 months
3

Change in albuminuria

Change in urine albumin-to-creatinine ratio from baseline to follow-up visits.

Time frame
Baseline, 12 months, and 24 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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