Development, Application, and Mechanistic Investigation of a Novel Minimally-Invasive Bidirectional Epidural Cerebellar Stimulation Technique for Cerebellar Cognitive Affective Syndrome

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

Building on previous findings regarding microglial immune function and the immunosuppressive effects of glucocorticoids, this project centers on the cerebellum's role in cognitive science. Using Cushing's syndrome-induced cerebellar atrophy leading to CCAS as a model, we aim to elucidate the pathogenic mechanisms governed by the neuro-adrenal-immune network and to uncover the molecular basis by which a novel minimally invasive brain-machine fusion system ameliorates cerebellar ataxia and cognitive impairment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
Healthy Volunteers: f
View:

• 1\. Clinically and biochemically confirmed ACTH-dependent or ACTH-independent Cushing syndrome (loss of serum cortisol circadian rhythm, elevated 24-hour urinary free cortisol, and failure to suppress on low-dose dexamethasone suppression test).

• 2\. Cranial MRI demonstrating unequivocal cerebellar atrophy (CCAS imaging criterion: cerebellar hemisphere or vermian volume ≥1.5 SD below age-matched normative data).

• 3\. Established clinical diagnosis of CCAS (meets Schmahmann criteria, CCAS-S total score ≥20).

• 4\. Cerebellar ataxia rating scale (SARATA) ≥10, indicating at least moderate motor ataxia.

• 5\. Positive cognitive impairment screen (MoCA \<26, or Z-scores ≤-1.5 in at least two cognitive domains).

• 6\. Willingness to undergo minimally invasive epidural cerebellar stimulation and provision of written informed consent.

Locations
Other Locations
China
Department of Urology, Peking University First Hospital, Beijing, 100034
RECRUITING
Beijing
Contact Information
Primary
Zheng Zhang
doczhz@aliyun.com
139 0137 1490
Time Frame
Start Date: 2025-06-28
Estimated Completion Date: 2028-06-01
Participants
Target number of participants: 200
Sponsors
Leads: Peking University First Hospital

This content was sourced from clinicaltrials.gov