Effect of Tenofovir (TDF) on Renal Function in Patients With Chronic Hepatitis B

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-60
SponsorAssiut University

About this trial

Effect of Long-Term Use of Tenofovir (TDF) on Renal Function in Patients with Chronic Hepatitis B Over a Five-Year Period

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial population

Study Population Age Range: 18 to 60 years Sex: Male and Female HBV Status: HBV-positive patients Treatment Duration: Long-term use of Tenofovir (TDF) for more than five years Sampling Method: Non-Probability Sampling Healthy Volunteers: Not Accepted

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Tenofovir Disoproxil Fumarate (TDF)

    Drug

    ANTIVIRAL TREATMENT FOR CHRONIC HEPATITIS B VIRUS INFECTION

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Changes in eGFR in Patients on Long-Term Tenofovir (TDF) Therapy

"Renal function will be assessed using estimated glomerular filtration rate (eGFR) calculated by the CKD-EPI equation

Time frame
BASELINE
2

Assessment of Renal Function: Serum Creatinine in Patients on Long-Term Tenofovir (TDF) Therapy

"Renal function will be assessed using serum creatinine levels measured through standard laboratory assays.

Time frame
BASELINE
3

proteinuria will be evaluated through urine protein-to-creatinine ratio

proteinuria will be evaluated through urine protein-to-creatinine ratio (if applicable).

Time frame
BASELINE

Secondary outcomes

Other outcomes

Sponsors and contacts

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