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Home/Company News/Conventus Completes Enrollment for European Study
Company News

Conventus Completes Enrollment for European Study

August 20, 2012 1 min read Premium comments

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Conventus Completes Enrollment for European Study
Conventus Orthoaedic Corporate Offices / Courtesy of Conventus Orthopaedic
Secondary

Conventus Orthopaedics, Inc., a Minneapolis, Minnesota, fracture fixation company, has completed enrollment for a clinical study of its Conventus DRS Implant for peri-articular fractures, according to an August 1 news release. The international multi-center clinical study has enrolled 60 patients from six institutions throughout Germany and Switzerland.

Conventus designed its implant to provide a less invasive means for orthopedic surgeons to treat patients with this traumatic injury, hoping to return them to normal daily activities sooner and with less pain.

Company officials say that the Conventus DRS technology provides clinicians with a self-expanding implant that stabilizes the fractured bone fragments from within the bone. The surgical procedure requires only a two to three centimeter incision on the forearm and a few small incisions distally.

The technique is claimed to reduce surgical trauma by as much as 70% compared to traditional plate and screws fixation and preserves soft tissues around the fracture to minimize stiffness, swelling, and pain. The developers believe that the DRS technology represents the first minimally-invasive, fragment-specific system that effectively addresses a wide range of fracture patterns with fixation strength as good as or better than traditional plates and screws.

A team of medical device professionals and physicians founded Conventus Orthopaedics, Inc. in 2008 to provide less invasive solutions to a broad range of challenging end-bone fractures. They took their name from the Latin word for coming together or union.

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Discussion

14
DS
Dr. Sarah MitchellOrthopedic Surgeon · Mayo Clinic

This is a fascinating development. In my practice we've seen similar outcomes with the revised protocol. The key differentiator seems to be patient selection criteria. Has anyone else noticed the correlation with BMI thresholds?

8
JT
James Thornton, MDSpine Fellow · HSS

Great point. I'd push back slightly on the conclusion, the sample size in the cited study is too small to draw population-level inferences. That said, the directional signal is compelling and worth a larger RCT.

5
RP
R. PatelSports Medicine · Stanford

We implemented a similar approach last year. Early results are promising but we're still gathering 12-month follow-up data. Happy to share our protocol if anyone is interested.

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