A Novel Oral Natural Extract for the Treatment of Senile Purpura

Status unconfirmed · Not applicable · Has a placebo group

Conditions studied: PURPURA

In brief

A randomized, double-blind, placebo controlled study to assess the safety and effectiveness of a novel oral natural extract to improve the appearance of the skin of patients with senile purpura.

Key facts

Study ID

NCT01183910

Run by

Nexgen Dermatologics, Inc.

People needed

75

Starts

2008-11-01

Expected to finish

2011-08-01

Last updated by the study team

2011-06-08

Who can join

Age: 40 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Patients with evidence of purpura on physical exam

You may not qualify if…

• Preexisting condition that would not allow the patients to take oral calcium supplement

Where it is running

• Berlin Center of Medical Aesthetics — Boynton Beach, Florida, United States

Full record on ClinicalTrials.gov

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