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Comparison of the Electric Plasma Surgical Tool PlasmaBlade for Replacement of the Deep Brain Stimulation (DBS) Devices With Conventional Surgery

Comparison of the Electric Plasma Surgical Tool PlasmaBlade for Replacement of the Deep Brain Stimulation (DBS) Devices With Conventional Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05535556
Enrollment
50
Registered
2022-09-10
Start date
2022-07-14
Completion date
2024-02-14
Last updated
2022-09-10

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

Conditions

Dystonia, Epilepsy, Essential Tremor, Parkinson Disease

Brief summary

The deep brain stimulation is surgical technique used for the Parkinson's disease, essential tremor, dystonia, epilepsy, and psychiatric diseases. A pulse generator or battery (implanted pulse generator, IPG) is a need for replacement every few years. In general, electric cautery(BOVIE), which is commonly used in surgery, cannot be used when the deep brain stimulation machine is inserted, so conventional tools such as scissors and knives are used for replacement surgery. However, in the process, damage to the machine may be inflicted by knives, scissors, etc., and in the worst case, the machine may be unusable, resulting in financial and human consumption. Plasma Blade is currently used for tissue incision and coagulation in Korea, and is the only insurance-recognized tool in Korea for the replacement surgery of a cardiovascular implantable electronic device (CIED). The deep brain stimulation machine has a structure very similar to that of the heart electronics. In addition, the plasma blade was used to replace the deep brain stimulation machine overseas.The safety is reported in the surgery, so the plasma blade deep brain stimulation machine has been replaced in Korea. The investigators would like to check the safety and effectiveness for use in surgery.

Interventions

None listed

Sponsors

Yonsei University
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
19 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Men and women over the age of 19 * Those who voluntarily agree to participate in this clinical trial and are willing to comply with the clinical trial protocol * Persons who have previously undergone deep brain stimulation for Parkinson's disease, essential tremor, dystonia, epilepsy, etc. * Those who need replacement of deep brain stimulation machine

Exclusion criteria

* Those who cannot be under general anesthesia

Design outcomes

Primary

MeasureTime frameDescription
Complications occurred during surgeryImmediately after surgeryEvaluate mechanical damage to the DBS machine immediately after surgery

Secondary

MeasureTime frameDescription
Surgical timeIntraoperativeCheck the time required for surgery
The occurrence of wound-related complicationsThe 1 day after surgery, 3 weeks after surgery, 6 months after surgerythe occurrence of short-term/long-term complications (hematoma, infection, wound spread, and changes in mechanical resistance values) the 1 day after surgery, 3 weeks after surgery, and 6 months after surgery

Countries

South Korea

Contacts

Primary ContactJin Woo Chang
JCHANG@yuhs.ac82-02-2228-2150

Outcome results

None listed

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