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Clinical Trials
EM-05-015029 Project LUBLIN
Physician & Study Coordinator
Study Coordinator
Monica Hosler, CRC
email:
Monica.Hosler@sluhn.org
phone: 484-658-4567
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Synopsis
A Multi-Center, Prospective, Open-label, Randomized, Study of 3M™ Topical Tissue Adhesive versus Commercially Available Tissue Adhesive for the Closure of Traumatic Lacerations and Surgical Incisions. Project LUBLIN.
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Eligibility Criteria
- Subject is at least 22 years of age
- Subject is willing and able to attend all scheduled study visits and abide by all study restrictions
- Subject has a single laceration that is ≤ 100 mm (10.0 cm) in length or up to 4 surgical incision(s), each ≤ 100 mm (10.0 cm) in length, defined as Class I or Class II wound(s) in which the use of a tissue adhesive (in combination with but not replacing deep dermal sutures, if applicable) is appropriate, including the following:
- surgical incision from a minimally invasive surgery
- low tension incision
- superficial laceration
- clean, traumatic laceration with edges that can be easily approximated
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