UVB Model Validation Study
Study Details
Study Description
Brief Summary
Single centre, subject and observer blinded, placebo controlled, cross-over study of the effect of oral ibuprofen and topical hydrocortisone-21-acetate on ultraviolet radiation (UVR) induced pain and inflammation in healthy volunteers conducted in two segments and using an intra-individual comparison of application areas.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
Phase 1 |
Detailed Description
Single centre, subject and observer blinded, placebo controlled, cross-over study of the effect of oral ibuprofen and topical hydrocortisone-21-acetate on ultraviolet radiation (UVR) induced pain and inflammation in healthy volunteers conducted in two segments and using an intra-individual comparison of application areas.
Subjects that signed the informed consent and are eligible to the study will be irradiated on the back to evaluate their individual minimal erythema doses (MEDs). Read out to determine MED will be done within 24 h after UVR.
A training session (without study medication) using the MED definition areas will be performed in order to introduce subjects to the testing and rating procedures.
Subjects will come in within 14 days of screening to start the first Segment of the study.
Eligible subjects will be randomised to receive either:
-
IB 600 mg, applied orally b.i.d., or
-
OP, applied orally b.i.d.
Allocation of topical treatment to these areas will be randomly assigned to:
-
PG, 15 μl/cm2 applied topically b.i.d., or
-
HC, 15 μl/cm2 applied topically b.i.d.
Defined areas will be irradiated with defined dosages of UVR. Assessment of hyperalgesia to heat and signs of inflammation (erythema, skin temperature) for all areas will be performed.
Subjects return within 4 to 11 days to the study site for the second segment of the study. Treatment allocation will be crossed-over and new treatment areas will be selected on the back.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Other: Group A Ibuprofen 600 mg (active comparator); Hydrocortisone 15 microl/cm2 (active comparator); Placebo Gel (placebo comparator) |
Drug: Ibuprofen, Hydrocortisone
Ibuprofen 600 mg film coated tablets, b.i.d., Hydrocortisone-21-acetate creme (25%) 15 microl/cm2 b.i.d.
|
Other: Group B Oral Placebo (placebo comparator), Hydrocortisone 15 microl/cm2 (active comparator); Placebo Gel (placebo comparator) |
Drug: Hydrocortisone
Hydrocortisone-21-acetate creme (25%) 15 microl/cm2 b.i.d.
|
Outcome Measures
Primary Outcome Measures
- Hyperalgesia to heat [72 h]
Secondary Outcome Measures
- Erythema, Skin temperature [72 h]
Eligibility Criteria
Criteria
Inclusion Criteria:
- healthy volunteers
Exclusion Criteria:
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | X-pert Med GmbH | Graefelfing | Bavaria | Germany | 82166 |
Sponsors and Collaborators
- X-pert Med GmbH
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- XPM-024