Octylseal Surgical Adhesive in General Surgery

Completed · Phase 4

Conditions studied: Wounds

In brief

The purpose of this study is to evaluate how surgical adhesive is used.

Key facts

Study ID

NCT01514383

Run by

Medline Industries

People needed

34

Starts

2012-01-01

Expected to finish

2012-10-01

Last updated by the study team

2019-05-07

Who can join

Age: 8 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Candidate for use of a topical surgical skin adhesive

You may not qualify if…

• Subjects with know sensitivity to topical surgical tissue adhesive products or degrading products (cyanoacrylates or formaldehyde)
• Subjects with a history of keloid formation, hypotension, insulin dependent diabetes mellitus, blood/clotting disorders, peripheral vascular diseases or hypertrophy history
• Subjects who present with a contraindications for product usage as per labeling
• A wound with evidence of active infection or gangrene or wounds of decubitus etiology
• Mucosal surfaces or across mucocutaneous junctions or skin that might be exposed to bodily fluids or with dense natural hair
• Subjects with known hypersensitivity to cyanoacrylate or formaldehyde

Where it is running

• Jersey City Medical Center — Jersey City, New Jersey, United States
• Wyckoff Hospital — New York, New York, United States

Full record on ClinicalTrials.gov

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