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NCT04008784 · ClinicalTrials.gov registry record

Improvement of Short Term Outcome of Mild to Moderate Atopic Dermatitis Using a Combination of Crisaborole and a Concomitant Topical Corticosteroid Over a 8 Week Period

A clinical trial of Atopic Dermatitis, sponsored by Clinical Research Center of the Carolinas.

Completed
Registry status
16
Enrollment target
1
Study location

NCT04008784 is a study of Atopic Dermatitis that has completed, run by Clinical Research Center of the Carolinas. The registered enrollment target is 16 participants, below the 609-participant average among 150 other Atopic Dermatitis trials with a reported enrollment target (97% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT04008784, a study of Atopic Dermatitis, has completed, sponsored by Clinical Research Center of the Carolinas.

COMPLETED
Registry status
16 participants
Enrollment target
1
Study location

Study Summary

This trial is a single-center two arm, open label observational prospective study, that will evaluate the safety and efficacy of crisaborole ointment, 2% alone compared to a combination therapy of crisaborole and a topical corticosteroid (Triamcinolone Acetonide Ointment, 0.1%) over a 8 week period for the treatment of mild to moderate atopic dermatitis.

Conditions Studied

Interventions

  • DRUG Crisaborole 2% Topical Application Ointment [EUCRISA]
  • DRUG Triamcinolone Acetonide 0.1% Ointment

Study Locations (1)

South Carolina

  • Clinical Research Center of the Carolinas - Charleston

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2019-09-16
Est. Completion 2020-09-08

What the Registry Record Tells You About NCT04008784

The ClinicalTrials.gov registry entry for NCT04008784 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 16 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 609-participant average among 150 other Atopic Dermatitis trials with a reported enrollment target (97% lower). The listed sponsor is Clinical Research Center of the Carolinas, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Atopic Dermatitis appearing as the primary indexed condition, and to 2 interventions - of which Crisaborole 2% Topical Application Ointment [EUCRISA] is the first listed.

NCT04008784 reports 1 study location spanning 1 distinct geographic area - top geographies include South Carolina.

Frequently Asked Questions

What is clinical trial NCT04008784 about?

NCT04008784 is a clinical study titled "Improvement of Short Term Outcome of Mild to Moderate Atopic Dermatitis Using a Combination of Crisaborole and a Concomitant Topical Corticosteroid Over a 8 Week Period". This trial is a single-center two arm, open label observational prospective study, that will evaluate the safety and efficacy of crisaborole ointment, 2% alone compared to a combination therapy of crisaborole and a topical corticosteroid (Triamcinolone Acetonide Ointment, 0.1%) over a 8 week period ...

What is the current status of trial NCT04008784?

This trial is currently completed. The enrollment target is 16 participants. The study started on 2019-09-16. Estimated completion is 2020-09-08.

What conditions does trial NCT04008784 study?

This clinical trial studies the following conditions: Atopic Dermatitis.

What interventions are being tested in trial NCT04008784?

The interventions under investigation include: Crisaborole 2% Topical Application Ointment [EUCRISA] (DRUG), Triamcinolone Acetonide 0.1% Ointment (DRUG).

Who is sponsoring clinical trial NCT04008784?

This trial is sponsored by Clinical Research Center of the Carolinas, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04008784 being conducted?

This trial has 1 study location across South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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