Comparison of Outcomes in Asleep & Awake DBS With a Directional Electrode

Status Active, not recruiting

Clinical Trial Summary

Clinical Trial Description

To compare the clinical outcome of patients with Parkinson's disease (PD) treated with directional deep brain (dDBS) stimulation undergoing subthalamic deep brain stimulation operation (STN-DBS) under general anesthesia versus local anesthesia. In awake group, 10 patients with Parkinson's disease were treated with St Jude Medical/Abbott Infinity DBS system, and the electrode implantation and testing were performed while the patients were awake. In asleep group, 14 patients with Parkinson's disease were treated with St Jude Medical/Abbott Infinity DBS system, and the electrode implantation were performed while the patients were under general anesthesia. The clinical outcome of the DBS treatment, possible adverse effects and the electrode placement will be compared within these two groups. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04287465
Study type	Observational
Source	Hospital District of Helsinki and Uusimaa
Contact
Status	Active, not recruiting
Phase
Start date	August 1, 2018
Completion date	December 31, 2025

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Comparison of Outcomes in Asleep and Awake DBS With a Directional Electrode

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms