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Percutaneous Cochlear Implantation: Implementation of Technique

Percutaneous Cochlear Implantation: Implementation of Technique

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01460823
Acronym
PCI-I
Enrollment
5
Registered
2011-10-27
Start date
2011-10-31
Completion date
2014-07-31
Last updated
2014-12-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hearing Loss

Keywords

Hearing loss, Cochlear Implantation, Image guided surgery

Brief summary

The investigators are studying a new way of doing cochlear implant surgery called Percutaneous Cochlear Implantation. In this surgery, instead of doing a mastoidectomy where about 30ml of bone is removed, the investigators use image-guided technology (similar to GPS systems used to guide automobile travel) to drill directly from the surface of the skull to the cochlea, removing less than 2ml of bone. To use this technique, three markers (or anchor screws) are screwed into the bone around the ear. Next, an x-ray of the head (called a CT scan) is taken. Using this CT scan, a path to the inner ear (cochlea) is planned and a drill guide (Microtable) is made that mounts on the anchor screws. A drill will be attached to the guide and used to drill a path from the surface of the skull to the inner ear (cochlea). The implant electrode will be threaded through this path. All of these procedures take place under general anesthesia.

Interventions

PROCEDUREPercutaneous Cochlear Implantation using image guided surgical techniques

Percutaneous Cochlear Implantation using image guided surgical techniques.

Sponsors

Vanderbilt University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* 18-80 year old patients undergoing cochlear implantation who are able to participate in the informed consent process. * Pre-operative CT scan of head performed as standard of care for cochlear implant work-up.

Exclusion criteria

* Patients with co-morbidities so severe that the potential additional operating room time is deemed to be too significant of an operative risk. This assessment is made by the local institutions pre-operative work-up. * History of allergic reaction/intolerance of local anesthesia and/or epinephrine. * History of allergic reaction to titanium. * Patients with severe anatomical abnormality of the temporal bone. * Patients with severe chronic ear disease for whom traditional mastoidectomy might offer benefit. * Females who are pregnant.

Design outcomes

Primary

MeasureTime frameDescription
Percentage of participants who underwent successful Cochlear Implantation Via Percutaneous MethodParticipants will be followed post operatively until their 1st follow up visit with surgeon which on average is 3 weeks after surgery.A successful percutaneous cochlear implantation is one where the facial nerve was not damaged during the procedure and the surgeon did not resort back to the standard implantation method. We will measure the percentage of participants who underwent successful cochlear implantation via the percutaneous method.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026