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Using this randomization approach, each volunteer has the same chance of being given either the new treatment or the placebo. Volunteers receive either the topical pharmaceutical composition of the present invention, for example, a microemulsion as described above in the formulation examples 1 to 5wherein the active agents consist of one or more known anti-inflammatory molecules, optionally containing one or more analgesic agents such as lidocaine (4) or placebo for an appropriate period with biological parameters associated with the indicated disease state or condition being measured at the beginning (baseline measurements before any treatment), end (after the final treatment), and at regular intervals during the study period.]