A newly, dedicated robotic system for (super)microsurgery can increase efficiency and precison of microsurgical skills.
ID
Bron
Verkorte titel
Aandoening
Free flap, reconstruction, lower extremity, microsurgery
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
The primary objective of this study is to demonstrate the clinically applicable use of robot-assistance in lower extremity free-flap reconstruction. The primary outcome is the quality of the anastomosis using Structured Assessment of Microsurgery Skills (SAMS).
Achtergrond van het onderzoek
Lower extremity reconstruction is a field of plastic surgery that aims to restoring/maintaining limb function as well as ensuring optimal cosmetic outcomes. Recent advances in plastic surgical technique as well as the introduction of microvascular free tissue transfer has revolutionized this field, allowing the salvage of limbs that would have otherwise been amputated. Free tissue transfer is often needed when there is significant soft tissue loss with exposed bone, tendon, and blood vessels. Currently this operation is done by hand, were the hand is the limiting factor performing this technique. In cooperation with the Technical University in Eindhoven, and Maastricht University Medical Center, a new robotic platform has been developed. The primary objective of this study is to demonstrate the clinically applicable use of robotic-assistance in lower extremity free-flap reconstruction.
Doel van het onderzoek
A newly, dedicated robotic system for (super)microsurgery can increase efficiency and precison of microsurgical skills.
Onderzoeksopzet
Primary and secondary outcomes will be assessed during (and after) surgery.
Onderzoeksproduct en/of interventie
Robotic-assisted anastomose of the artery/veins/nerves of the free flap to reconstruction site
Publiek
Wetenschappelijk
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
- Any patient (>18 years or older) with an indication of lower extremity free-flap reconstruction.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
- Unable to provide informed consent (i.e. mentally unwell)
- Individual may not complete follow up for any reason.
- Patients younger than 18 years of age
Opzet
Deelname
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