A Feasibility Study of a Modular Video Augmentation System for Image-Guided Skull Base Surgery

Johns Hopkins Medicine

Status: Terminated

Conditions: Feasibility of Video Augmentation System; Value of Video Augmentation Navigation

Treatments: Device: Video Augmentation

Study type: Interventional

Funder types: Other

Identifiers

NCT01591954

J11101

NA_00051786 (Other Identifier)

Details and patient eligibility

About

Current standard of care for complex head, neck and skull base surgery require navigation systems that allow instruments to be tracked optically or electromagnetically while registered to a patient's pre-operative X-ray computed tomography (CT) or magnetic resonance image (MRI). However, conventionally, the CT/MRI data is not registered with video endoscopy. Augmentation of endoscopic video by preoperative data can facilitate navigation around critical structures and robust target resection. The work presented here describes evaluation of a high definition (HD) video-overlay system for endonasal endoscopic skull base surgery. We adopt a modular design that can be extended for other video augmentation applications. The system supports fast automatic camera calibration, comparable in re-projection errors to standard camera calibration tools, while performing within appropriate run time for clinical use. Phantom studies have shown the registration accuracy of the system to be equivalent to that of conventional optical tracking. With this system we are proposing a clinical pilot study in a small number of patients at Johns Hopkins Hospital to evaluate basic feasibility and to gather qualitative assessment of the video augmentation system.

Enrollment: 1 patient

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Participants must be at least 18 years of age or older;
• Have an existing clinically ordered CT image within 2 weeks of the study; or
• Have an existing clinically ordered MR image within 2 weeks of the study;
• Provide written informed consent after receiving a verbal and written explanation of the purpose and nature of this clinical study;
• Be able to communicate effectively with clinical study personnel

Exclusion criteria

• Major medical or psychiatric illness which, in the investigator's opinion, would prevent completion of the procedure;

Trial design

1 participants in 1 patient group

Video Augmentation

Experimental group

Description:

Qualitative assessment of the value of video-based navigation system

Treatment:

Device: Video Augmentation