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UVB-311nm After Initial Slow Response to Adalimumab in Psoriasis

Primary Purpose

Psoriasis

Status
Unknown status
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
UVB-311nm
No treatment
Sponsored by
Medical University of Graz
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Psoriasis focused on measuring Psoriasis, Biologic, adalimumab, narrowband UVB, phototherapy, half-side comparison

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Psoriasis patients with PASI reduction of less than 75% after at least 6 weeks of treatment with adalimumab.

Exclusion Criteria:

  • Pregnancy or lactation
  • History of skin cancer
  • Presence of or history of malignant skin tumors
  • Dysplastic melanocytic nevus syndrome
  • Antinuclear antibodies (ds-DNA, Ro/SSA, La/SSB)
  • Autoimmune disorders such as Lupus erythematosus or Dermatomyositis
  • Photosensitive diseases such as porphyria, chronic actinic dermatitis, Xeroderma pigmentosum, basal cell nevus syndrome, and others
  • General poor health status

Sites / Locations

  • Medical University of Graz, Department of DermatologyRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

left/right

Arm Description

left or right body side

Outcomes

Primary Outcome Measures

Modified PASI (psoriasis area and severity index)

Secondary Outcome Measures

VAS patient score for therapeutic effect
VAS patient score for severity of skin lesions

Full Information

First Posted
March 12, 2008
Last Updated
October 31, 2013
Sponsor
Medical University of Graz
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1. Study Identification

Unique Protocol Identification Number
NCT00638469
Brief Title
UVB-311nm After Initial Slow Response to Adalimumab in Psoriasis
Official Title
Prospective, Randomized Half-side Study on the Efficacy of UVB-311nm Phototherapy in Patients With Psoriasis After Partial Remission to Treatment With Adalimumab
Study Type
Interventional

2. Study Status

Record Verification Date
October 2013
Overall Recruitment Status
Unknown status
Study Start Date
March 2008 (undefined)
Primary Completion Date
December 2014 (Anticipated)
Study Completion Date
December 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical University of Graz

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Adalimumab, a fully human anti-tumor necrosis factor (TNF) monoclonal antibody has been approved for the treatment of moderate to severe psoriasis. However, in a portion of cases adalimumab does not induce reduction of psoriasis area and severity index (PASI) of 75% or greater, now being considered as gold standard for treatment efficacy. In this study we aim to determine in a randomized half-side comparison whether additional narrowband UVB-311nm phototherapy accelerates and improves the clearance of psoriatic lesions in adalimumab-treated patients after initial slow response.
Detailed Description
Patients with moderate to severe psoriasis who have received treatment with adalimumab (loading dose of 80 mg and thereafter 40 mg s.c. biweekly) for at least 6 weeks without a PASI reduction of 75% or greater qualify for the study. Adalimumab is continued and UVB-311nm phototherapy is added at 6 weeks or thereafter one a randomized body half (left or right; head exempt) 3 x per week until complete response (defined as reduction in PASI to < 3) for a maximum of another 6 weeks (until week 12). PASI score, visual analogue score (VAS) patient score for therapeutic response, and VAS patient score for severity of skin lesions is assessed weekly; and at follow-up visits at month 3, 6, and 12. Paired Wilcoxon testing for differences in PASI and patient VAS scores is done; Fischer exact test is applied to determine differences in complete remission, PASI reduction > 90%, > 75% and/or 50% between body sites.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psoriasis
Keywords
Psoriasis, Biologic, adalimumab, narrowband UVB, phototherapy, half-side comparison

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
10 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
left/right
Arm Type
Other
Arm Description
left or right body side
Intervention Type
Radiation
Intervention Name(s)
UVB-311nm
Other Intervention Name(s)
narrow-band UVB radiation
Intervention Description
UVB-311nm radiation given 3 times a week to one randomized body half
Intervention Type
Other
Intervention Name(s)
No treatment
Intervention Description
no UV exposure
Primary Outcome Measure Information:
Title
Modified PASI (psoriasis area and severity index)
Time Frame
12 months
Secondary Outcome Measure Information:
Title
VAS patient score for therapeutic effect
Time Frame
12 months
Title
VAS patient score for severity of skin lesions
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Psoriasis patients with PASI reduction of less than 75% after at least 6 weeks of treatment with adalimumab. Exclusion Criteria: Pregnancy or lactation History of skin cancer Presence of or history of malignant skin tumors Dysplastic melanocytic nevus syndrome Antinuclear antibodies (ds-DNA, Ro/SSA, La/SSB) Autoimmune disorders such as Lupus erythematosus or Dermatomyositis Photosensitive diseases such as porphyria, chronic actinic dermatitis, Xeroderma pigmentosum, basal cell nevus syndrome, and others General poor health status
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Peter Wolf, MD
Phone
+43 316 385
Ext
80315
Email
peter.wolf@medunigraz.at
First Name & Middle Initial & Last Name or Official Title & Degree
Angelika Hofer, MD
Phone
+43 316 385
Ext
80315
Email
angelika.hofer@medunigraz.at
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Wolf, MD
Organizational Affiliation
Medical University of Graz, Austria
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical University of Graz, Department of Dermatology
City
Graz
ZIP/Postal Code
A-8036
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Peter Wolf, MD
Phone
+43 316 385
Ext
80315
Email
peter.wolf@medunigraz.at
First Name & Middle Initial & Last Name & Degree
Angelika Hofer, MD
Phone
+43 316 385
Ext
13254
Email
angelika.hofer@medunigraz.at
First Name & Middle Initial & Last Name & Degree
Peter Wolf, MD
First Name & Middle Initial & Last Name & Degree
Angelika Hofer, MD
First Name & Middle Initial & Last Name & Degree
Franz Legat, MD
First Name & Middle Initial & Last Name & Degree
Wolfgang Salmhofer, MD
First Name & Middle Initial & Last Name & Degree
Alexandra Gruber-Wackernagel, MD
First Name & Middle Initial & Last Name & Degree
Wolfgang Weger, MD

12. IPD Sharing Statement

Learn more about this trial

UVB-311nm After Initial Slow Response to Adalimumab in Psoriasis

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