Investigating markers in children with sudden-onset neuropsychiatric symptoms
Official title: Neurobiologic, Immunologic, and Rheumatologic Markers in Youth With PANS
Run by Stanford University · NCT02889016 · Data updated 2026-11-12
This study is testing if certain biological markers in children with sudden neuropsychiatric symptoms can help us understand Pediatric Acute-Onset Neuropsychiatric Syndrome (PANS) better.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 4 Years to 18 Years |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | Stanford University Academic / other |
| Locations | 1 site (Palo Alto, California) |
| Status | Recruiting |
| Started | March 2013 |
| Main results expected | March 2028 |
| Study ends | March 2028 |
| Registry record updated | October 6, 2016 |
| Trial ID | NCT02889016 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are children aged 1-18 who have recently been diagnosed with PANS and live within 90 miles of Stanford University.
✕Probably not a fit
Patients with other neuropsychiatric illnesses that could complicate the diagnosis of PANS may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to explore the neurologic, immunologic, and rheumatologic markers in children diagnosed with Pediatric Acute-Onset Neuropsychiatric Syndrome (PANS). The study will recruit 500 children aged 1-18 who have experienced a recent onset of PANS symptoms, and these participants will be compared to 100 healthy age- and gender-matched controls. By examining various biological components, the research seeks to uncover underlying mechanisms associated with PANS, which may be triggered by infections or inflammation. The findings could provide insights into the condition and inform future treatment strategies.
Why it matters
Potential benefit: If successful, this study could lead to a better understanding of PANS and improve diagnostic and treatment approaches for affected children.
How similar studies have gone: While this study explores a specific aspect of PANS, similar studies have shown promise in understanding autoimmune and neuropsychiatric disorders, indicating potential for success.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Children with PANS 1. Age 1-18 at onset of PANS 2. Diagnosis of PANS: abrupt onset of OCD or food restriction, and at least two of the following associated symptoms: frequent urination, worsening handwriting/cognition, inattention, anorexia, separation anxiety, oppositionality, irritability/rage outbursts, and emotional lability. 3. Patients must live within 90 miles of Stanford University and have a new onset of PANS illness 4. Patients must have an established pediatrician within 90 miles of Stanford University for 3 years. * Healthy Controls 1. Age 4-18 2. No psychiatric diagnosis Exclusion Criteria: * Any neuropsychiatric illness that may obscure the clear diagnosis of PANS
Where it's running
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Stanford University
Palo Alto, California, United States Recruiting
Study contacts
- Study coordinator: Joanne Cheung
- Email: pansresearch@stanford.edu
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Biomarkers for PANS: Diagnosing and Tracking Pediatric Neuropsychiatric Symptoms
This study tests a panel of biomarkers to help diagnose PANS in children and see if they reflect disease course and response to treatment.
-
Study on Pediatric Autoimmune Neuropsychiatric Disorders Linked to Streptococcus
This study is looking at how common certain neuropsychiatric disorders are in children aged 3-17 and how they might be linked to a specific type of bacteria called Group A streptococcus.
-
Evaluating patterns in neurodevelopmental disorders
This study is trying to find common signs and causes of neurodevelopmental disorders like Autism and Down Syndrome to help with earlier diagnosis and better outcomes for those affected.
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A platform for collecting health data on ME/CFS and Long Covid
This study is trying to collect health information from adults with ME/CFS and Long Covid to help researchers better understand these conditions and improve future treatments.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.