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

NCT00121511 · ClinicalTrials.gov registry record · NA

The Effect of Efudex Treatment on Photoaged Skin

A NA study, sponsored by University of Michigan.

Completed
Registry status
NA
Development phase
21
Enrollment target

NCT00121511: Completed NA study, sponsored by University of Michigan.

NCT00121511 is a NA study that has completed, run by University of Michigan. The registered enrollment target is 21 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00121511, a NA study, has completed, sponsored by University of Michigan.

COMPLETED
Registry status
NA
Development phase
21 participants
Enrollment target

Study Summary

The researchers propose that skin improvements may be seen following a course of Efudex, (5-fluorouracil), a FDA-approved topical therapy (applied directly to the skin). These improvements could be the result of both a reduction of actinic keratoses (small red horny growths or flesh-colored wartlike growths caused by overexposure to ultraviolet radiation or the sun) and improvement of sun-damaged skin. In addition, this research study is being done to determine if the expression of p53, a tumor suppressor gene (its activity stops the formation of tumors), is decreased following Efudex treatment. Mutations (abnormal changes) in the gene, called p53, are associated with a certain type of skin cancer. In addition, p53-mutated genes are known to exist in non-cancerous sun-damaged skin. Thus, the presence of p53 mutations may serve as a marker for both sun damage and an elevated risk of developing skin cancer.

Interventions

  • DRUG Efudex (5-fluorouracil)

Trial Details

FieldValue
Enrollment Target 21 participants
Start Date 2005-07
Est. Completion 2007-07
Phase NA
University of Michigan

1,327 total trials

What the finished NCT00121511 record still lists

NCT00121511 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 21 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which Efudex (5-fluorouracil) is the first listed.

NCT00121511 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00121511 about?

NCT00121511 is a clinical study titled "The Effect of Efudex Treatment on Photoaged Skin". The researchers propose that skin improvements may be seen following a course of Efudex, (5-fluorouracil), a FDA-approved topical therapy (applied directly to the skin). These improvements could be the result of both a reduction of actinic keratoses (small red horny growths or flesh-colored wartlike...

What is the current status of trial NCT00121511?

This trial is currently completed. It is a NA study. The enrollment target is 21 participants. The study started on 2005-07. Estimated completion is 2007-07.

What interventions are being tested in trial NCT00121511?

The interventions under investigation include: Efudex (5-fluorouracil) (DRUG).

Who is sponsoring clinical trial NCT00121511?

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 NCT00121511's enrollment target sits among peer trials

21 1762nd of 2000 higher than 233 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

  • NCT02447874 · 21 participants · Phase 1

    Arginine Therapy for the Treatment of Pain in Children With Sickle Cell Disease

  • NCT03826992 · 21 participants · Phase 1

    Venetoclax Combined With Vyxeos (CPX-351) for Participants With Relapsed or Refractory Acute Leukemia

  • NCT04107077 · 21 participants · Phase 2

    Phase II Study of the Effects of Laparoscopic Hyperthermic Intraperitoneal Chemotherapy (HIPEC) in Patients With Advanced Gastric Cancer

  • NCT04158635 · 21 participants · Phase 1

    Gemcitabine, Nab-Paclitaxel, and Bosentan for the Treatment of Unresectable Pancreatic 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 NCT00121511, the US trial registry maintained by the National Library of Medicine. NCT00121511 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.