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Clinical Trials/EUCTR2004-004466-33-DE
EUCTR2004-004466-33-DEActive, not recruitingNot Applicable

doubleblind (observer blind), placebo-controlled, clinical-experimental study phase II in order to examine the local compatibility of Dr. Theiss Ringelblumen Salbe N by the duhring-chamber-test and in a open user trial - local compatibility test and open user trial with Dr. Theiss Ringelblumen Salbe

Dr. Theiss Naturwaren GmbH0 sites40 target enrollmentStarted: January 9, 2006Last updated:
Conditions
Drugs

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Enrollment
40

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional clinical trial of medicinal product

Eligibility Criteria

Sex
All

Inclusion Criteria

  • •written informed consent written informed data protection healthy subjects with healthy normal skin conditions age more than 18 years
  • •Are the trial subjects under 18? no
  • •Number of subjects for this age range:
  • •F.1.2 Adults (18-64 years) yes
  • •F.1.2.1 Number of subjects for this age range
  • •F.1.3 Elderly (>=65 years) no
  • •F.1.3.1 Number of subjects for this age range

Exclusion Criteria

  • •Volunteers who do not fulfill any of the above described criteria Volunteers who are pregnant or breast feeding Skin irritation or disease Skin dieseases or dermatological disorders Volunteeers with severe disorders Topical medication in the test areas Participation in an study in the last 4 weeks Consumption of alcohol or drugs

Investigators

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