Actively Recruiting

Age: 18Years - 85Years
All Genders
NCT07166432

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

Led by Peking University First Hospital · Updated on 2025-09-10

200

Participants Needed

1

Research Sites

152 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Clinically and biochemically confirmed ACTH-dependent or ACTH-independent Cushing syndrome
  • Cranial MRI showing cerebellar atrophy with volume 1.5 SD below age norms
  • Established clinical diagnosis of Cerebellar Cognitive Affective Syndrome (CCAS) with CCAS-S total score 20 or higher
  • Cerebellar ataxia rating scale (SARATA) score of 10 or more indicating moderate motor ataxia
  • Positive cognitive impairment screen with MoCA below 26 or Z-scores -1.5 or less in at least two cognitive areas
  • Willingness to undergo minimally invasive epidural cerebellar stimulation and provide written informed consent
Not Eligible

You will not qualify if you...

  • Significant systemic disease
  • Major complications or critical deviations in data or procedures
  • Clinical deterioration, serious adverse events, or poor compliance making continued participation inappropriate

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Urology, Peking University First Hospital, Beijing, 100034

Beijing, China

Actively Recruiting

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Research Team

Z

Zheng Zhang

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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