Actively Recruiting

Phase 4
Age: 18Years +
All Genders
Healthy Volunteers
NCT04376216

Prednisolone Treatment in Acute Interstitial Nephritis

Led by Region MidtJylland Denmark · Updated on 2020-12-30

110

Participants Needed

1

Research Sites

521 weeks

Total Duration

On this page

Sponsors

R

Region MidtJylland Denmark

Lead Sponsor

A

Aarhus University Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

A Prospective randomized trial with a primary objective to investigate the effect ofprdenisolone treatment in acute interstitial nephritis

CONDITIONS

Official Title

Prednisolone Treatment in Acute Interstitial Nephritis

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Biopsy confirmed acute interstitial nephritis (AIN)
  • Clinical suspicion of AIN
  • Age over 18 years
  • Either plasma creatinine greater than 120 µmol/L or an increase in plasma creatinine greater than 30 µmol/L or more than 50% increase from baseline
  • Fertile women are eligible
Not Eligible

You will not qualify if you...

  • Unable to provide informed consent
  • Immunosuppressive treatment including prednisolone within 3 months before biopsy
  • Presence of autoimmune disease
  • Intolerance to prednisolone
  • Pregnancy or breastfeeding
  • Active cancer except basal cell carcinoma
  • Life expectancy less than 6 months
  • Chronic kidney disease stage IV or V
  • AIN caused by or accompanied by glomerulonephritis, sarcoidosis, or inherited interstitial kidney disease
  • Previous participation in this study
  • Development of exclusion criteria during study
  • Withdrawal of consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Godstrup Hospital

Herning, Denmark, 7400

Actively Recruiting

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Research Team

F

Frank Mose, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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