Efficacy and Safety of Fibrin Sealant (FS) VH S/D-APR for Hemostasis and Wound Healing in Endoscopic Browlift

Status unconfirmed

Conditions studied: Compare Ecchymosis and Edema for Fibrin Sealant and no Fibrin Sealant

In brief

The primary objective is to evaluate the safety and efficacy of Artiss (Fibrin Sealant) in reducing the incidence of early postoperative bruising and swelling.

Key facts

Study ID

NCT01320514

Run by

Nguyen, Davis B., M.D.

People needed

10

Starts

2010-12-01

Expected to finish

2011-05-01

Last updated by the study team

2011-03-22

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Subjects planned for endoscopic browlift, subjects who read, understand and sign the written informed consent, healthy female or male subjects, 18-75 years old, and subjects who are able and willing to comply with the protocal requirements

You may not qualify if…

• Subjects who had previous browlift, subjects indicated for concurrent facial surgeries, subjects considered to be active smokers, subjects with ecchymosis/edema on day 0, significant laboratory abnormalities, subjects with known bleeding or coagulation disorders, subjects treated with anti-coagulants.

Where it is running

• Davis B Nguyen, M.D. — Beverly Hills, California, United States (enrolling)

Full record on ClinicalTrials.gov

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