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Senior Design Project: Stent-Saver Eva Bica Dominique Gonzalez George Collard Rebecca Gonter Joseph Grogan
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Our Solution
- A Remotely-Operated Stitching Device
- Consists of three parts
- Proximal Device
- Front part to be inserted into patient to place spiral clips
- Connection
- Tube containing several tubes within it
- Distal Device
- Back end to be hand operated

Breakdown Of Parts
- Proximal Device
- Delivers Nitinol Clips
- Telescoping series of tubes
- Four Tubes:
- Tube 1: outermost, hard polyurethane
- Tube 2: hard/springy nitinol bend (120 degrees)
- Tube 3: soft straight nitinol, inner profile is oval, needle at top
- Tube 4: innermost, soft polyurethane screw. Oval shape, which prevents nitinol clips from rotating, forcing them to translate upward Material: Nitinol and Polyurethane

- Connection System
- Translates Operation of Distal Device to Proximal Movement
- Concentric Tubes
- Material: Polyurethane

- Distal Device
- Hand-Held / Operated
- 2 Dials, 2 Sliders
- Internal Mechanisms Link Movements
- Constructed of:
- Plastic Casing and dials/sliders
- Nylon and steel gears
- Tubes pushed by sliders
- Tubes rotated by dials
- Gears link backwards motion of slider to rotation of screw

Nitinol Clip Information
- Purpose of clip
- To secure stent-graft to aorta wall
- To prevent leakage and slippage
- Clip Selection
- Oval spiral shape chosen because it had the strongest overallsupport
- A series of clips will be placed to ensure safety and symmetry
- Nitinol selected as material (FDA approved)
- Clips are oriented in criss-cross manner to ensure a tighter hold

  
Material Selection
- Nitinol
- Nickel Titanium alloy has shape memory properties (after being heated in a shape, that shape is retained)
- Can undergo large elastic deformation

- Polyurethane
- Unique material that offers the elasticity of rubber combined with the toughness and durability of metal
- Urethanes have better abrasion and tear resistance than rubbers, while offering higher load bearing capacity
- FDA approved
- Compatible with human body
Reason for Development
- To eliminate or greatly reduce the need for open surgery, which is very traumatic to the body
- To increase the success rate of endovascular surgery over time
- Providing a simple, safe, effective solution to the problem of leakage and slippage of endovascular stent-grafts
- Patient saves money due to less follow up visits and eliminates need for additional procedures
 
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©2004. Eva Bica, Dominique Gonzalez, George Collard, Rebecca Gonter, Joseph Grogran.
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