Assessment of OviTex devices in breast reconstruction surgeryResearch Question:
Does breast reconstruction using OviTex lead to fewer complications compared to surgeries
that do not use OviTex?
Basic Study Information
Purpose:Location: Stong Memorial Hospital
The purpose of this research is to collect data related to OviTex used in breast reconstructions
to help determine if the use of OviTex in breast reconstructions leads to fewer complications
than breast reconstructions performed without the use of OviTex. Data will be collected
from enrolled patients 12 and 24 months after surgery. Patients 18-79 years old at
the time of surgery are eligible for this study. At the time of surgery, the patient
must have received an OviTex PRS Permanent (R20143, R20243, or R30343) or Resorbable
(R20152 or R20252) implant in conjunction with and implant-based breast reconstruction.
Study Reference #: STUDY00007323
Lead Researcher (Principal Investigator)
Study Contact InformationStudy Coordinator: Colleen Casey
Phone: (937) 514-2262
Additional Study Details
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