Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02467075 · ClinicalTrials.gov registry record · Phase 4

Double-Blind Placebo-Controlled CIN Trial

A Phase 4 study, sponsored by University of Michigan.

Terminated
Registry status
Phase 4
Development phase
1
Enrollment target

NCT02467075: Clinical Trial Phase 4 study, sponsored by University of Michigan.

NCT02467075 is a Phase 4 study that was terminated before completion, run by University of Michigan. The registered enrollment target is 1 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (100% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02467075, a Phase 4 study, was terminated before completion, sponsored by University of Michigan.

TERMINATED
Registry status
Phase 4
Development phase
1 participants
Enrollment target

Study Summary

This double-blinded placebo-controlled study will examine the incidence and significance of contrast-induced acute kidney injury following IV iodine-based contrast material administration in subjects with stage IIIB or stage IV chronic kidney disease. Subjects will be scheduled for clinically indicated CT of the abdomen and/or pelvis to evaluate for suspected intra-abdominal infection. Subjects will be randomized to receive either weight-based low-osmolality iodinated contrast material or saline. The primary outcome measure will be the incidence of stage II AKI by AKIN (Acute Kidney Injury Network) criteria.

Primary Outcome

Participants who had Stage II AKI. This is measured by comparing an initial blood creatinine level with the level at 48 hours. Creatine is a chemical waste product that passes through the kidneys. Creatinine levels reflect how well the kidneys are working.

Interventions

  • DRUG Placebo (Normal Saline)
  • DRUG Iopamidol 300 (Contrast)

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2015-07
Est. Completion 2015-09
Phase Phase 4
University of Michigan

1,327 total trials

Why NCT02467075 stopped before completion

NCT02467075 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 1 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (100% lower).

The record links to 0 conditions, and to 2 interventions - of which Placebo (Normal Saline) is the first listed.

NCT02467075 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02467075 about?

NCT02467075 is a clinical study titled "Double-Blind Placebo-Controlled CIN Trial". This double-blinded placebo-controlled study will examine the incidence and significance of contrast-induced acute kidney injury following IV iodine-based contrast material administration in subjects with stage IIIB or stage IV chronic kidney disease. Subjects will be scheduled for clinically indic...

What is the current status of trial NCT02467075?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 1 participants. The study started on 2015-07. Estimated completion is 2015-09.

What interventions are being tested in trial NCT02467075?

The interventions under investigation include: Placebo (Normal Saline) (DRUG), Iopamidol 300 (Contrast) (DRUG).

Who is sponsoring clinical trial NCT02467075?

This trial is sponsored by University of Michigan, which has 1,327 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02467075's enrollment target sits among peer trials

1 2000th of 2000 the lowest of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT02467075, the US trial registry maintained by the National Library of Medicine. NCT02467075 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.