Optic Nerve Sheath Fenestration
1 other identifier
interventional
20
1 country
1
Brief Summary
The purpose of this study is to develop a way to perform safer surgery in the eye socket. The eye and its surrounding structures are very delicate and can easily be damaged from surgery. A laser may act as a gentle knife to cut the tissue. Currently, this is done with a small scissors and knife, but it could be done with gentle laser. By using an endoscope, the surgery could be much safer and faster. Vanderbilt has a Free Electron Laser, which could be used to make a small hole in the coverings around the optic nerve to treat certain diseases. Before it is used in seeing eyes, the laser must be tested on eyes which are to be removed during an enucleation to prove that it does not damage the optic nerve The standard enucleation (removal of your blind painful eye) will be performed. This procedure will be performed at the Free Electron Laser Center Operating Room, which is a fully equipped operating room currently being used for outpatient surgery. The post-operative recovery room setting is similar to the post-operative recovery room in the previously used area. This includes general anesthesia with a breathing tube in your throat, injecting an anesthetic liquid behind the eye for comfort after surgery, and removing the eyeball. Enucleations must be performed under general anesthesia or intravenous sedation with a retrobulbar injection (injection behind the eye). The anesthesiologist will determine which is safer to perform. The removed globe will be replaced with a spherical implant. Just prior to the removal of the eyeball, a small opening will be made in the coverings around your optic nerve (the cable exiting the eyeball) with the endoscopic laser or with a knife and scissors. The procedure should not take much longer than the standard eye removal. The procedure will be identical to the standard enucleation (eye removal) except for making the tiny hole in the coverings of the optic nerve, which should take about 15 to 30 minutes. The laser is very tissue specific. It only reacts with certain types of tissue and should not damage the surrounding tissue. There will be no additional costs to you associated with the study portion of the procedure.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jul 2000
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2000
CompletedFirst Submitted
Initial submission to the registry
June 16, 2006
CompletedFirst Posted
Study publicly available on registry
June 20, 2006
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2006
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2006
CompletedJanuary 8, 2013
January 1, 2013
6.4 years
June 16, 2006
January 6, 2013
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Histologic Evaluation
Measured at time of procedure
Ease of Procedure
At time of procedure
Histological Evaluation
At time of procedure
Interventions
Eligibility Criteria
You may qualify if:
- Blind Eye Needing Enucleation
You may not qualify if:
- Capable of being performed at FEL Surgical OR
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Vanderbilt Universitylead
- United States Department of Defensecollaborator
Study Sites (1)
Vanderbilt University
Nashville, Tennessee, 37232, United States
Study Officials
- STUDY DIRECTOR
Sandy A Owings, COA, CCRP
Vanderbilt University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor of Ophthalmology
Study Record Dates
First Submitted
June 16, 2006
First Posted
June 20, 2006
Study Start
July 1, 2000
Primary Completion
December 1, 2006
Study Completion
December 1, 2006
Last Updated
January 8, 2013
Record last verified: 2013-01