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

NCT00890968 · ClinicalTrials.gov registry record · Phase 2

Safety and Efficacy Study of Triamcinolone Acetonide DuraPeel to Treat Hand Dermatitis

A Phase 2 study, sponsored by ZARS Pharma.

Completed
Registry status
Phase 2
Development phase
56
Enrollment target

NCT00890968 is a Phase 2 study that has completed, run by ZARS Pharma. The registered enrollment target is 56 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00890968, a Phase 2 study, has completed, sponsored by ZARS Pharma.

COMPLETED
Registry status
Phase 2
Development phase
56 participants
Enrollment target

Study Summary

The purpose of this study is to determine whether Triamcinolone Acetonide (TAC) DuraPeel is safe and effective in the treatment of hand dermatitis.

Interventions

  • DRUG Triamcinolone Acetonide (TAC) DuraPeel
  • DRUG Placebo DuraPeel

Trial Details

FieldValue
Enrollment Target 56 participants
Start Date 2009-04
Est. Completion 2009-08
Phase Phase 2

Sponsor

ZARS Pharma

23 total trials

What the Registry Record Tells You About NCT00890968

The ClinicalTrials.gov registry entry for NCT00890968 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 56 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is ZARS Pharma, which has 23 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Triamcinolone Acetonide (TAC) DuraPeel is the first listed.

NCT00890968 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00890968 about?

NCT00890968 is a clinical study titled "Safety and Efficacy Study of Triamcinolone Acetonide DuraPeel to Treat Hand Dermatitis". The purpose of this study is to determine whether Triamcinolone Acetonide (TAC) DuraPeel is safe and effective in the treatment of hand dermatitis.

What is the current status of trial NCT00890968?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 56 participants. The study started on 2009-04. Estimated completion is 2009-08.

What interventions are being tested in trial NCT00890968?

The interventions under investigation include: Triamcinolone Acetonide (TAC) DuraPeel (DRUG), Placebo DuraPeel (DRUG).

Who is sponsoring clinical trial NCT00890968?

This trial is sponsored by ZARS Pharma, which has 23 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.