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

NCT01469767 · ClinicalTrials.gov registry record · Phase 2

Efficacy of Fluocinonide Cream 0.1% (Vanos(R)) in Reducing Itch in Subjects With Atopic Dermatitis

A Phase 2 study, sponsored by Wake Forest University.

Completed
Registry status
Phase 2
Development phase
10
Enrollment target

NCT01469767: Completed Phase 2 study, sponsored by Wake Forest University.

NCT01469767 is a Phase 2 study that has completed, run by Wake Forest University. The registered enrollment target is 10 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT01469767, a Phase 2 study, has completed, sponsored by Wake Forest University.

COMPLETED
Registry status
Phase 2
Development phase
10 participants
Enrollment target

Study Summary

The purpose of this study is to assess the efficacy of short-term treatment with fluocinonide cream 0.1% (Vanos®) in the treatment of atopic dermatitis (AD).

Primary Outcome

Investigator's Global Assessment of atopic dermatitis integrates all lesions for overall score. This measure is commonly used to quantify disease severity and most resembles assessments performed in the clinic setting. Score ranges from '0' = Clear to '5' = Very Severe Disease

Interventions

  • DRUG Fluocinonide cream

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2012-02-01
Est. Completion 2013-08-17
Phase Phase 2
Wake Forest University

100 total trials

What the finished NCT01469767 record still lists

NCT01469767 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (92% lower).

The record links to 0 conditions, and to 1 intervention - of which Fluocinonide cream is the first listed.

NCT01469767 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01469767 about?

NCT01469767 is a clinical study titled "Efficacy of Fluocinonide Cream 0.1% (Vanos(R)) in Reducing Itch in Subjects With Atopic Dermatitis". The purpose of this study is to assess the efficacy of short-term treatment with fluocinonide cream 0.1% (Vanos®) in the treatment of atopic dermatitis (AD).

What is the current status of trial NCT01469767?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 10 participants. The study started on 2012-02-01. Estimated completion is 2013-08-17.

What interventions are being tested in trial NCT01469767?

The interventions under investigation include: Fluocinonide cream (DRUG).

Who is sponsoring clinical trial NCT01469767?

This trial is sponsored by Wake Forest University, which has 100 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01469767's enrollment target sits among peer trials

10 1968th of 2000 higher than 12 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

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

  • NCT00623389 · 10 participants · NA

    Evaluation of an Advanced Lower Extremity Neuroprostheses

  • NCT01241864 · 10 participants · Phase 2

    Islet Transplantation in Type 1 Diabetic Kidney Allograft

  • NCT01293214 · 10 participants · NA

    Vascularized Composite Allotransplantation for Multiple Extremity Amputations

  • NCT01474148 · 10 participants · NA

    A Neuroprosthesis for Seated Posture and Balance

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT01469767, the US trial registry maintained by the National Library of Medicine. NCT01469767 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.