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Sponsored by: |
Northwestern University |
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Information provided by: | Northwestern University |
ClinicalTrials.gov Identifier: | NCT00363038 |
The primary objective of this study is to determine the efficacy of different topical ointments compared with placebo for the resolution of post-laser induced bruising.
Condition | Intervention |
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Ecchymosis |
Drug: Vitamin K Drug: Vitamin K and Retinol Drug: Arnica |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Single Group Assignment |
Official Title: | Effects of Topical Vitamin K, Vitamin K and Retinol, and Arnica on Post-Laser Bruising |
Enrollment: | 15 |
Study Start Date: | August 2006 |
Estimated Study Completion Date: | July 2007 |
The primary purpose of this study is to determine the efficacy of different topical ointments compared with placebo for the resolution of post-laser induced bruising.
Ages Eligible for Study: | 20 Years to 60 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
United States, Illinois | |
Northwestern Memorial Hospital | |
Chicago, Illinois, United States, 60611 |
Principal Investigator: | Murad Alam, MD | Northwestern University |
Study ID Numbers: | 1253-015 |
Study First Received: | August 10, 2006 |
Last Updated: | October 12, 2007 |
ClinicalTrials.gov Identifier: | NCT00363038 |
Health Authority: | United States: Institutional Review Board; United States: Food and Drug Administration |
Signs and Symptoms Antiplasmin Contusions Retinol palmitate |
Vitamin A Vitamin K Ecchymosis Hemorrhage |
Skin Manifestations Molecular Mechanisms of Pharmacological Action Coagulants Growth Substances Physiological Effects of Drugs Hematologic Agents Pharmacologic Actions |
Hemostatics Fibrin Modulating Agents Pathologic Processes Antifibrinolytic Agents Therapeutic Uses Vitamins Micronutrients |