Trial of Treatment of Atopic Dermatitis With Concurrent Altabax® and Topical Low-Potency Corticosteroids Versus Low-Potency Corticosteroid Mono-therapy

This study has been withdrawn prior to enrollment.
(Funding withdrawn)
Sponsor:
Collaborator:
GlaxoSmithKline
Information provided by:
St. Luke's-Roosevelt Hospital Center
ClinicalTrials.gov Identifier:
NCT00871208
First received: March 27, 2009
Last updated: June 29, 2010
Last verified: June 2010

March 27, 2009
June 29, 2010
May 2009
May 2010   (final data collection date for primary outcome measure)
Superiority of drug to vehicle in reducing Eczema Area and Severity Index (EASI) scores in children with atopic dermatitis [ Time Frame: Each patient will be enrolled for a 4 week trial ] [ Designated as safety issue: No ]
Superiority of drug to vehicle in reducing EASI scores in children with atopic dermatitis [ Time Frame: Each patient will be enrolled for a 4 week trial ] [ Designated as safety issue: No ]
Complete list of historical versions of study NCT00871208 on ClinicalTrials.gov Archive Site
Improved quality of life with usage of the drug altabax (R) and topical corticosteroids over vehicle and topical corticosteroids for treatment of atopic dermatitis in children with atopic dermatitis. [ Time Frame: 4 week trial of medication ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Trial of Treatment of Atopic Dermatitis With Concurrent Altabax® and Topical Low-Potency Corticosteroids Versus Low-Potency Corticosteroid Mono-therapy
Randomized, Placebo-Controlled Trial of Treatment of Atopic Dermatitis With Concurrent Altabax® and Topical Low-Potency Corticosteroids vs. Low-Potency Corticosteroid Mono-therapy

This study is designed to determine whether the addition of topical Altabax (R) to a treatment regimen of topical corticosteroid therapy speeds clearance of atopic dermatitis and improves quality of life.

Background: Atopic dermatitis is a pruritic skin disorder which affects more than 10% of the United States population, one-third of whom report sleep disturbance and a quarter with chronic unremitting disease. Atopic dermatitis is a recurrent pruritic skin disorder which has a significant morbidity and extensive costs for the health care system. Quality of life is often impaired for patients with atopic dermatitis due to sleep disturbance, pruritus and the physical impairment of visible skin lesions.

The rapidity in which pruritus and lesional appearance are noted to resolve correlates strongly with improved patient satisfaction and improved quality of life.

Recently, a clinical trial of adding mupirocin into a regimen of topical corticosteroids has shown a significant enhancement in lesional clearance and symptom reduction with addition of mupirocin to the topical corticosteroid. These improvements were most notable within the first week of treatment.

Proposal: A 4-week clinical trial of 60 atopic dermatitis patients (ages 9 months to 17 years) would be conducted. All sixty patients would be given topical mid-potency corticosteroid (Locoid lipocream®) to be mixed with a second product. Half the patients would receive Altabax® and the other half would receive vehicle (blinded to subject and investigator). Patients would be advised to apply the topical randomized product first, let dry and then apply topical Locoid lipocream ® to affected areas, and then apply the topical randomized ointment product to each of the sites of skin disease on top of the Locoid lipocream ®. Treatment of affected areas would continue for 4 weeks or until lesions have cleared, which ever comes first. Parents of patients will be asked to maintain a written diary of drug application.

Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator)
Primary Purpose: Treatment
Atopic Dermatitis
  • Drug: Altabax (R)
    Retapamulin 1% ointment is to be applied to lesional atopic dermatitis twice-daily in addition to a topical corticosteroid (Locoid lipocream (R))
    Other Names:
    • Altabax(R)ointment
    • Locoid lipocream (R)
  • Drug: Vehicle and Locoid lipocream (R)
    The vehicle base of retapamulin ointment will be applied twice-daily to active lesions of atopic dermatitis in addition to locoid lipocream (R)
    Other Name: Locoid lipocream (R)
  • Experimental: 1
    Altabax (R) and Locoid Lipocream (R):Patients will apply both drugs sequentially to active lesions of atopic dermatitis. Physical examination, skin cultures, photos and quality of life scores will be performed at baseline, week 1, week 2 and week 4.
    Intervention: Drug: Altabax (R)
  • Active Comparator: 2
    Vehicle and Locoid Lipocream (R):Patients will apply both drugs sequentially to active lesions of atopic dermatitis. Physical examination, skin cultures, photos and quality of life scores will be performed at baseline, week 1, week 2 and week 4.
    Intervention: Drug: Vehicle and Locoid lipocream (R)

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Withdrawn
60
May 2010
May 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Diagnosis of Atopic Dermatitis
  2. Ages 9 months to 17 years
  3. Presence of at least one lesion of atopic dermatitis at the time of baseline enrollment
  4. Disease limited to less than 100 cm2 body surface area
  5. EASI Score of at least 7, based on the Gong, et al publication Gong JQ, Lin L, Lin T, Hao F, Zeng FQ, Bi ZG, Yi D, Zhao B. Skin colonization by Staphylococcus aureus in patients with eczema and atopic dermatitis and relevant combined topical therapy: a double-blind multicentre randomized controlled trial. Br J Dermatol. 2006 Oct;155(4):680-7.

Exclusion Criteria:

  1. Allergy to any ingredient in Altabax® or Locoid lipocream ®
  2. Usage of oral corticosteroids within the 2 weeks prior to study initiation or during the study
  3. Usage of topical corticosteroid or other topical prescriptions for atopic dermatitis in the week prior to study initiation
  4. Inability to comply with the study protocol
  5. Presence of major medical illness requiring systemic therapy including cancers.
  6. Clinical diagnosis of bacterial infections of the skin, including impetigo or abscesses.
Both
9 Months to 17 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00871208
SLR08-057-111672
Yes
Nanette Silverberg, MD, St. Luke's-Roosevelt Hospital Center
St. Luke's-Roosevelt Hospital Center
GlaxoSmithKline
Not Provided
St. Luke's-Roosevelt Hospital Center
June 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP