Explorative study: the relevance of contact allergy to isobornyl acrylate in people with an other acrylate allergy

Completed

• Conditions: allergic contact dermatitis; contact eczema; 10014982

• Registration Number: NL-OMON35745
• Lead Sponsor: niversitair Medisch Centrum Groningen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 6 May 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 20

Inclusion Criteria

- Adulthood
- Legal competence
- Epicutanous skin test in the UMCG between 01-01-2000 and 01-02-2012
- Positive reaction (at least +) for at least one acrylate

Exclusion Criteria

- Legally incompetence
- Angry back in the past
- Active skin disease on the back
- Use of immunosuppresive drugs
- Pregnancy(wish)

Study & Design

• Study Type: Observational invasive
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>The primary study parameters are the results of the patch tests. These will be<br /><br>scored following the guidelines of the International Contact Dermatitis<br /><br>Research Group (ICDRG).The responses are qualified as -, +? , +, ++, +++ or IR<br /><br>(irritation) response. The +, ++ and +++ will be translate in 1 and relevant<br /><br>for our study, while -, +? and IR will be translated into 0 and will be<br /><br>considered negative.<br /><br>Besides the scores, we will also take pictures of the back. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>n.a.</p><br>