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Assessment of OviTex devices in breast reconstruction surgery

Research Question:
Does breast reconstruction using OviTex lead to fewer complications compared to surgeries that do not use OviTex?

Basic Study Information

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.

Location: Stong Memorial Hospital
Study Reference #: STUDY00007323

Lead Researcher (Principal Investigator)

Lead Researcher:  Gui Christiano

Study Contact Information

Study Coordinator: Colleen Casey
Phone: (937) 514-2262

Additional Study Details

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