Actively Recruiting
NeuroCytotron in the Treatment of Autism Spectrum Disorder
Led by Neurocytonix, Inc. · Updated on 2025-02-06
100
Participants Needed
1
Research Sites
63 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Preliminary Efficacy and Feasibility of Using NeuroCytotron in the Treatment of Autism Spectrum Disorder
CONDITIONS
Official Title
NeuroCytotron in the Treatment of Autism Spectrum Disorder
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Male or female subjects with a confirmed diagnosis of ASD according to DSM-5 criteria
- Age between 3 and 50 years
- ASD severity grade 1 to 3 according to DSM-5 criteria
- Informed consent provided by parents or legal representatives
- Physically able and willing to participate in treatment sessions
- Medically and psychologically stable for study participation
You will not qualify if you...
- Medical conditions contraindicating NeuroCytotron use, including severe neurological disorders
- Uncontrolled epilepsy defined as more than 1 generalized seizure per month in the past 3 months
- History of prolonged or repetitive seizures requiring rescue medication within 9 months
- Participation in other autism therapies during the study
- Logistical or situational issues preventing regular attendance
- History of significant adverse reactions to similar treatments or anesthesia
- Serious behavioral problems or aggression affecting safety
- Current or recent (within 14 days) significant infection
- Presence of magnetic implants, pacemakers, claustrophobia, or conditions preventing NeuroCytotron use
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
NeuroCytonix México
San Pedro Garza García, Nuevo León, Mexico, 66224
Actively Recruiting
Research Team
K
Karen Camarillo Cardenas
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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