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

NCT00478439 · ClinicalTrials.gov registry record · Phase 4

Investigation of Macular Pigment Augmentation on Dark Adaptation

A Phase 4 study, sponsored by University of Alabama at Birmingham.

Terminated
Registry status
Phase 4
Development phase
13
Enrollment target

NCT00478439: Clinical Trial Phase 4 study, sponsored by University of Alabama at Birmingham.

NCT00478439 is a Phase 4 study that was terminated before completion, run by University of Alabama at Birmingham. The registered enrollment target is 13 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00478439, a Phase 4 study, was terminated before completion, sponsored by University of Alabama at Birmingham.

TERMINATED
Registry status
Phase 4
Development phase
13 participants
Enrollment target

Study Summary

The study will evaluate whether taking a nutritional supplement designed to increase macular pigment in the eye can improve a person's ability to adjust to darkness. Patients will be assigned to take either a placebo or nutritional supplement for 8 months. Vision will be assessed at baseline, 4 months, and 8 months.

Interventions

  • DIETARY_SUPPLEMENT Multivitamin
  • DIETARY_SUPPLEMENT ZeaVision EyePromise Restore

Trial Details

FieldValue
Enrollment Target 13 participants
Start Date 2007-12
Est. Completion 2010-10
Phase Phase 4
University of Alabama at Birmingham

1,160 total trials

Why NCT00478439 stopped before completion

NCT00478439 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 13 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 2 interventions - of which Multivitamin is the first listed.

NCT00478439 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00478439 about?

NCT00478439 is a clinical study titled "Investigation of Macular Pigment Augmentation on Dark Adaptation". The study will evaluate whether taking a nutritional supplement designed to increase macular pigment in the eye can improve a person's ability to adjust to darkness. Patients will be assigned to take either a placebo or nutritional supplement for 8 months. Vision will be assessed at baseline, 4 mont...

What is the current status of trial NCT00478439?

This trial is currently terminated. It is a Phase 4 study. The enrollment target is 13 participants. The study started on 2007-12. Estimated completion is 2010-10.

What interventions are being tested in trial NCT00478439?

The interventions under investigation include: Multivitamin (DIETARY_SUPPLEMENT), ZeaVision EyePromise Restore (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT00478439?

This trial is sponsored by University of Alabama at Birmingham, which has 1,160 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00478439's enrollment target sits among peer trials

13 1910th of 2000 higher than 88 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 enrollment target

  • NCT03125655 · 13 participants

    Regulation of Inflammatory Genes in Psoriasis

  • NCT03774446 · 13 participants · Phase 2

    Multicenter Study of Seliciclib (R-roscovitine) for Cushing Disease

  • NCT03830151 · 13 participants · Phase 1

    Hyperpolarized Carbon C 13 Pyruvate in Diagnosing Glioma in Patients With Brain Tumors

  • NCT04573231 · 13 participants · Phase 2

    Evaluation of PSMA in HER2- AR+ Metastatic Breast Cancer

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 NCT00478439, the US trial registry maintained by the National Library of Medicine. NCT00478439 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.