Frontlight ResearchEarly access
TerminatedPhase 4
Trial of Naproxen Sodium for the Treatment of OCD in Children With PANDAS
Key facts
- Who runs it
- Massachusetts General Hospital
- Where
- Boston, United StatesSee the site
- Trial code
- Status
- Terminated
- Phase
- Phase 4
- People taking part
- 2 people enrolled
- Started
- 20 Oct 2020
- Ended
- 30 Apr 2025
- Type of study
- Interventional, 2 groupsOne group gets a placebo (a dummy treatment), for comparison.
- Treatments tested
- Naproxen Sodium
- Placebo
- Record updated
- 20 May 2026
- Why it stopped
- Low recruitment
Who can take part
- Age
- 6 years to 15 years
- Sex
- Women and men
- Healthy volunteers
- Cannot take part
The registry criteria, word for word
Show all 29 criteriaShow less
Who can take part
- significantly interfering Obsessive-Compulsive Disorder (OCD) symptoms
- ages 6- to 15-years-old
- new-onset of OCD symptoms within the previous 18 months
- sufficient fluency of English to understand study staff, procedures and questionnaires,
- able to take medication in pill form
- parent/legal guardian who can provide informed consent; Patients must also meet all criteria for PANDAS, which are:
- prepubertal symptom onset
- acute onset of symptoms (from no/minimal symptoms to maximum severity within 24-48 hours) and/or an episodic (relapsing-remitting) course
- temporal association between symptomatic periods and infections with Group A Streptococcus (GAS) infection
- presence of neurological abnormalities (e.g. handwriting deterioration, choreiform movements); The onset/exacerbation of OCD symptoms must also be accompanied by at least three of the following clinical signs and symptoms, including:
- Markedly increased level of anxiety, particularly new onset of separation anxiety
- Emotional lability, irritability, aggressive behavior and/or personality change
- Sudden difficulties with concentration or learning
- Developmental regression ("baby-talk", temper tantrums)
- Sleep disorder (insomnia, night terrors, refusal to sleep alone)
- Handwriting deterioration or other sign of motoric dysfunction (including new onset of motor hyperactivity, presence of choreiform finger movements, pronator drift or truncal instability)
- Urinary frequency or increased urge to urinate; daytime or night-time secondary enuresis; These co-occurring symptoms must be "severe" or "dramatic" and proceed from no/minimal symptoms to maximum severity within the same 24-48 hour interval during which the OCD symptoms arose. In addition to these inclusion criteria, PANDAS subjects will be required to provide documentation of a positive GAS infection via medical records. As the time between a documented GAS infection and the onset of PANDAS symptoms has not been defined in the PANDAS diagnostic criteria, the investigators will use a guideline of approximately six weeks or less between a documented GAS infection and the onset of OCD symptoms for inclusion into the study
Who cannot take part
- concurrent antibiotic treatment or antibiotic treatment within one-week of baseline
- concurrent selective serotonin reuptake inhibitor (SSRI) or other psychoactive medication treatment except and unless the dose has been stable for at least 6 weeks (i.e. no recent titration, initiation, or change in dosage)
- concurrent medications that do not meet the above criteria (e.g., other psychotropic medications or anti-inflammatory agents)
- child has a serious neurological disorder or impairment (e.g. brain damage, blindness, deafness), an intellectual disability, or autism
- history of immune modulating therapies for OCD/PANDAS symptoms
- history of ulcers in the digestive system
- history of restricted fluid intake, as this could exacerbate side effects
- history of severe asthma or currently uncontrolled asthma
- pre-existing liver, kidney, GI bleeding or clotting disorders (GFR <75 mL/min/1.73m2)
- child who is acutely psychotic or suicidal
- pregnant or becomes pregnant
- currently engaged in an intensive outpatient cognitive behavioral treatment program (more than weekly)
Where in United States
- Massachusetts General HospitalBoston, United States
About the trial
What the trial wants to find out
This project aims to rigorously evaluate a potential treatment for inflammation-related Obsessive-Compulsive Disorder (OCD) symptoms in children. To accomplish this goal, the investigators will conduct a double-blind, randomized, placebo-controlled trial of Naproxen Sodium, a nonsteroidal anti-inflammatory drug (NSAID) in participants diagnosed with Pediatric Autoimmune Neuropsychiatric Disorder Associated with Streptococcal infections (PANDAS). This research fills a gap in the empirical evidence base for the treatment of PANDAS, and will add to a growing literature of empirically-derived practices for PANDAS.
The 2 groups in the trial
- InterventionTreatment being tested
Participants receive Naproxen Sodium.
Treatment: Naproxen Sodium
- PlaceboPlacebo, for comparison
Participants receive placebo.
Data and sources
- Registry record
- Listed on ClinicalTrials.gov.
- Official title
- Double-Blind, Randomized, Placebo-Controlled Trial of Naproxen Sodium for the Treatment of Obsessive Compulsive Symptoms in Pediatric Autoimmune Neuropsychiatric Disorder Associated With Streptococcal Infections (PANDAS)
- Record updated
- 20 May 2026