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NCT00004448 · ClinicalTrials.gov registry record · Phase 2

Alternate Day Prednisone or Daily Fish Oil Supplements in Patients With Immunoglobulin A Nephropathy

A Phase 2 study, sponsored by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).

Completed
Registry status
Phase 2
Development phase
96
Enrollment target

NCT00004448: Completed Phase 2 study, sponsored by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).

NCT00004448 is a Phase 2 study that has completed, run by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK). The registered enrollment target is 96 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (28% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00004448, a Phase 2 study, has completed, sponsored by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK).

COMPLETED
Registry status
Phase 2
Development phase
96 participants
Enrollment target

Study Summary

OBJECTIVES: Evaluate the efficacy of alternate day prednisone versus daily fish oil supplements in slowing or preventing the decline in renal function in children, adolescents, and young adults with moderate to severe immunoglobulin A nephropathy.

Primary Outcome

Time to failure was defined as the interval until the eGFR fell to \<60% of baseline value.

Interventions

  • DRUG Placebo
  • DRUG prednisone
  • DRUG omega-3 fatty acids

Trial Details

FieldValue
Enrollment Target 96 participants
Start Date 1997-11
Est. Completion 2007-08
Phase Phase 2

What the finished NCT00004448 record still lists

NCT00004448 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 96 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (28% lower).

The record links to 0 conditions, and to 3 interventions - of which Placebo is the first listed.

NCT00004448 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00004448 about?

NCT00004448 is a clinical study titled "Alternate Day Prednisone or Daily Fish Oil Supplements in Patients With Immunoglobulin A Nephropathy". OBJECTIVES: Evaluate the efficacy of alternate day prednisone versus daily fish oil supplements in slowing or preventing the decline in renal function in children, adolescents, and young adults with moderate to severe immunoglobulin A nephropathy.

What is the current status of trial NCT00004448?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 96 participants. The study started on 1997-11. Estimated completion is 2007-08.

What interventions are being tested in trial NCT00004448?

The interventions under investigation include: Placebo (DRUG), prednisone (DRUG), omega-3 fatty acids (DRUG).

Who is sponsoring clinical trial NCT00004448?

This trial is sponsored by National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK), which has 490 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00004448's enrollment target sits among peer trials

96 747th of 2000 higher than 1,242 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00004448, the US trial registry maintained by the National Library of Medicine. NCT00004448 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.