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Study identifier: NCT07176494 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Revision of Deep Brain Stimulator in Patients With Parkinson's Disease

Condition: Pain Management · Regional Anesthesia · Deep Brain Stimulation  ·  Sponsor: Ankara Etlik City Hospital

PhaseNA
Planned participants50
Who can joinAll sexes, 40 Years to 85 Years
Healthy volunteersNo

About this study

Parkinson's disease is a chronic and progressive neurodegenerative disease that affects the central nervous system, particularly impairing movement control. It is associated with the loss of dopamine-producing cells in the brain and typically occurs in middle age and beyond. Deep brain stimulation (DBS) is considered when symptoms of Parkinson's disease, such as tremors, slowed movements, and muscle rigidity, are not adequately controlled with medications. Selected patients with severe symptoms that do not respond to medical treatment are generally considered for this treatment. Battery revision surgeries can be performed under general anesthesia or regional anesthesia. Patients undergoing general anesthesia should be cautious about the potential complications of general anesthesia, while those undergoing regional anesthesia should be cautious about the local anesthetic systemic toxicity. Because each method has its own advantages, the choice of anesthesia may vary. This study aimed to compare postoperative analgesic efficacy and patient satisfaction in patients who underwent surgery under general anesthesia or sedation-assisted battery replacement under regional anesthesia. Both anesthesia methods are routinely used in Parkinson's disease patients undergoing battery replacement.

This description comes directly from the study's public registry record.

Talk to the study team

İbrahim MD Topcu, MD  ·  05437860316  ·  ibrahimtpc78@gmail.com

Musa MD Zengin  ·  +905307716235  ·  musazengin@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Ankara Etlik City HospitalAnkara, Yenimahalle\Ankara, Turkey (Türkiye)Recruiting

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Source record: clinicaltrials.gov/study/NCT07176494