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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
Trial of Naproxen Sodium for the Treatment of OCD in Children With PANDAS (NCT04015596) – Frontlight Research