Skip to main content
Clinical Trials/NL-OMON45591
NL-OMON45591
Not yet recruiting
Not Applicable

Identification of inflammatory mediator profiles associated with dental devices in order to provide leads in detecting an oral allergic reaction. - Skingiva Study

Academisch Centrum Tandheelkunde Amsterdam0 sites50 target enrollmentStarted: TBDLast updated:

Overview

Phase
Not Applicable
Status
Not yet recruiting
Enrollment
50

Overview

Brief Summary

No summary available.

Study Design

Study Type
Observational invasive

Eligibility Criteria

Ages
18 to 64 (—)

Inclusion Criteria

  • In order to be eligible to participate in this study, a subject must meet all of the following criteria:
  • \* Patients suspected of having an allergic reaction to palladium or nickel in their dental restorative material and who are orally exposed to these metals by their dental devices and who are scheduled to receive a routine skin patch test at the outpatient clinic Dermato\-allergology \& occupational dermatology at the VU University Medical Centre for diagnosis of nickel and palladium allergy.
  • \* Patients must be willing to undergo crevicular fluid collection, venipuncture and skin adhesive tape stripping

Exclusion Criteria

  • A potential subject who meets any of the following criteria will be excluded from participation in this study:
  • \* Pregnancy or lactation
  • \* Age under 18 or above 80
  • \* Smoking, no more than ten cigarettes per day
  • \* Legally incompetent adults
  • \* Usage of systemic immunosuppressive drugs (e.g. prednison, acitretine, adalimumab, efalizumab, etanercept, methoxsaleen, cyclosporine, azathioprine, infliximab and methothrexate) and antibiotics at least 2 weeks prior to starting of the study NB: Medication that reasonably not intervenes with the study procedures (e.g. an antihistaminicum can be used during the study)
  • \* Severe disorders within the last 6 month, e.g. cancer, acute cardiac\- and circularity disorders, serious diabetics
  • \* Participation in a study with pharmaceutical within a period of at least 4 weeks prior to this study
  • \* Immunological disorders, e.g. HIV, infectious hepatitis,
  • \* Alcohol and drug abuse

Investigators

Similar Trials