Apremilast and Moderate to Severe Chronic Hand Dermatitis

Part of paid clinical trials in Washington D.C., District of Columbia.

Sponsor
George Washington University
Study ID
NCT03741933
Phase
PHASE4
Status
Withdrawn

Conditions

  • Chronic Hand Dermatitis

Eligibility Criteria

Sex
ALL
Age
18 Years - 79 Years
Healthy Volunteers
Accepted

Interventions

Study Details

Investigators have designed a pilot study involving chronic hand dermatitis (CHD) patients who attend the dermatology clinic at the George Washington Medical Faculty Associates (GW MFA) in order to assess the efficacy and safety of apremilast treatment for the treatment of moderate to severe CHD.

Key Dates

First listed
Nov 15, 2018
Start date
Feb 28, 2019
Status verified
Jan 2023
Primary completion
Aug 1, 2019
Completion
Aug 1, 2019

Study Design

Enrollment
0 participants (actual)
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT

Arms

  • Experimental: Apremilast
    30 mg twice daily to be administered for a period of 6 months

Primary Outcome Measure

To evaluate the efficacy of Apremilast 30mg twice daily administered as monotherapy in the treatment of moderate-to-severe CHD as assessed by improvement of the Physician Global Assessment (PGA). [ Time Frame: 24 weeks ]

Locations (1)

FacilityCityStateZIPSite coordinators
George Washington University Department of DermatologyWashington D.C.District of Columbia20037-

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