Clinical Prediction Model for Disease Progression in Primary Membranous Nephropathy

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

About this trial

This prospective observational study aims to evaluate predictors of disease progression in patients with primary membranous nephropathy and to assess the performance of a prognostic nomogram in predicting renal outcomes in the Egyptian population.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years

Biopsy-proven primary membranous nephropathy

Written informed consent

Disqualifiers

Secondary membranous nephropathy (e.g., lupus nephritis, hepatitis B or C, malignancy, drug-induced)

Pregnancy

End-stage kidney disease at presentation

Refusal to participate

Trial population

Adults with biopsy-proven primary membranous nephropathy attending the Nephrology Unit, Department of Internal Medicine, Assiut University Hospitals who meet the eligibility criteria.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Performance of the prognostic nomogram in predicting disease progression

Ability of the prognostic nomogram to predict disease progression in patients with primary membranous nephropathy, assessed by the area under the receiver operating characteristic curve (AUC).

Time frame
6 months

Secondary outcomes

1

Independent clinical and laboratory predictors of disease progression

Identification of independent clinical and laboratory predictors of disease progression in primary membranous nephropathy using multivariable analysis

Time frame
6 months
2

Decline in estimated glomerular filtration rate (eGFR)

Change in estimated glomerular filtration rate (eGFR) from baseline, measured in mL/min/1.73 m².

Time frame
6 months
3

Remission status

Proportion of patients achieving complete or partial remission according to KDIGO criteria

Time frame
6 month
4

Validation of the prognostic nomogram

Validation of the predictive performance of the prognostic nomogram in the local patient population using discrimination and calibration metrics

Time frame
6 months

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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