Effects of Neuralli® MP on Self-Defined Outcomes in Adults With Autistic Traits (NCT07064538) | Clinical Trial Compass
Active — Not RecruitingNot Applicable
Effects of Neuralli® MP on Self-Defined Outcomes in Adults With Autistic Traits
Taiwan15 participantsStarted 2025-08-19
Plain-language summary
To evaluate the efficacy of Neuralli® MP in improving participant-defined outcomes in adults with autistic traits.
Who can participate
Age range
18 Years – 50 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Participants aged between 18 and 50 who exhibit autistic traits
* Those who have the willingness and ability to work but have not yet been able to enter a sheltered workshop at the Kanner Foundation
* The subjects, primary caregivers and institution staff are willing to participate in the study, and the primary caregivers and institution staff are willing to fill out the questionnaire and accept the interview
Exclusion Criteria:
* Those who have taken antibiotics or probiotic products in powder, capsule or tablet form within the past month are excluded.
* Participants currently receiving antibiotic treatment are also excluded.
* Individuals with a known allergy to dairy products.
* Individuals with immunodeficiency or compromised immune function.
* Individuals diagnosed with small intestinal bacterial overgrowth (SIBO)
* Ineligibility determined by PI, e.g. the individual starts any new medication or therapy, especially related to their autism, during this time.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.