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Trial of Naproxen Sodium for the Treatment of OCD in Children With PANDAS

Primary Purpose

PANDAS, Anxiety Disorder, Autoimmune Diseases

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Naproxen Sodium
Placebo
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for PANDAS focused on measuring PANDAS, Children, Obsessive-Compulsive Disorder, Anxiety, NSAID

Eligibility Criteria

6 Years - 15 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. significantly interfering Obsessive-Compulsive Disorder (OCD) symptoms
  2. ages 6- to 15-years-old
  3. new-onset of OCD symptoms within the previous 18 months
  4. sufficient fluency of English to understand study staff, procedures and questionnaires,
  5. able to take medication in pill form
  6. parent/legal guardian who can provide informed consent.

Patients must also meet all criteria for PANDAS, which are:

  1. prepubertal symptom onset
  2. acute onset of symptoms (from no/minimal symptoms to maximum severity within 24-48 hours) and/or an episodic (relapsing-remitting) course
  3. temporal association between symptomatic periods and infections with Group A Streptococcus (GAS) infection
  4. 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:

  1. Markedly increased level of anxiety, particularly new onset of separation anxiety
  2. Emotional lability, irritability, aggressive behavior and/or personality change
  3. Sudden difficulties with concentration or learning
  4. Developmental regression ("baby-talk", temper tantrums).
  5. Sleep disorder (insomnia, night terrors, refusal to sleep alone)
  6. Handwriting deterioration or other sign of motoric dysfunction (including new onset of motor hyperactivity, presence of choreiform finger movements, pronator drift or truncal instability)
  7. 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.

Exclusion Criteria:

  1. child who is acutely psychotic or suicidal
  2. child has a serious neurological disorder or impairment (e.g. brain damage, blindness, deafness), an intellectual disability, or autism
  3. history of immune modulating therapies for OCD/PANDAS symptoms
  4. pre-existing liver, kidney, GI bleeding or clotting disorders (GFR <75 mL/min/1.73m2)
  5. history of ulcers in the digestive system
  6. history of restricted fluid intake, as this could exacerbate side effects
  7. concurrent antibiotic treatment or antibiotic treatment within one-week of baseline
  8. pregnant or becomes pregnant
  9. currently engaged in an intensive outpatient cognitive behavioral treatment program (more than weekly)
  10. 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)
  11. concurrent medications that do not meet the above criteria (e.g., other psychotropic medications or anti-inflammatory agents)
  12. history of severe asthma or currently uncontrolled asthma

Sites / Locations

  • Massachusetts General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Intervention

Placebo

Arm Description

Participants receive Naproxen Sodium.

Participants receive placebo.

Outcomes

Primary Outcome Measures

Children's Yale-Brown Obsessive-Compulsive Scale, 2nd Edition (CY-BOCS-II)
The CY-BOCS-II is a clinician-rated measure to assess obsessive-compulsive symptom severity. This results in two subscale total scores, Obsessions and Compulsion, each ranging from 0-25, with a higher score indicating more symptom severity. These subscale scores are summed to provide a total score, ranging from 0 to 50, that is used to measure overall OCD symptom severity.
Children's Yale-Brown Obsessive-Compulsive Scale, 1st Edition (CY-BOCS-I)
The CY-BOCS-I is a clinician-rated measure to assess obsessive-compulsive symptom severity. This results in two subscale total scores, Obsessions and Compulsion, each ranging from 0-20, with a higher score indicating more symptom severity. These subscale scores are summed to provide a total score, ranging from 0 to 40, that is used to measure overall OCD symptom severity.

Secondary Outcome Measures

Changes in C reactive protein pre- and post-treatment between groups
C reactive protein (CRP, mg/L) will be obtained from pre- and post-blood draws and will be compared between groups.
Changes in erythrocyte sedimentation rate pre- and post-treatment between groups
Erythrocyte sedimentation rate (ESR, mm/h) will be obtained from pre- and post-blood draws and will be compared between groups.

Full Information

First Posted
June 11, 2019
Last Updated
March 23, 2023
Sponsor
Massachusetts General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04015596
Brief Title
Trial of Naproxen Sodium for the Treatment of OCD in Children With PANDAS
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)
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
October 20, 2020 (Actual)
Primary Completion Date
October 31, 2024 (Anticipated)
Study Completion Date
October 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes

5. Study Description

Brief Summary
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.
Detailed Description
The investigators propose to systematically evaluate the effects of naproxen sodium on anti-obsessional and behavioral improvement and conduct the first randomized controlled trial of naproxen sodium in the treatment of children with PANDAS. The study will involve an 8-week, double-blinded randomized controlled trial to evaluate the efficacy of naproxen sodium (10mg/kg, by mouth, twice a day) versus placebo to treat OCD symptoms in children with PANDAS. The investigators will acquire completed data on 44 children with PANDAS for this pilot study (i.e., 22 randomized to active treatment; 22 randomized to placebo). Outcome will be assessed comparing pre- and post-treatment OCD symptom severity using a standardized, clinician-administered interview assessing OCD symptoms by an independent rater blind to treatment assignment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
PANDAS, Anxiety Disorder, Autoimmune Diseases, Obsessive-Compulsive Disorder
Keywords
PANDAS, Children, Obsessive-Compulsive Disorder, Anxiety, NSAID

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
70 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
Participants receive Naproxen Sodium.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Participants receive placebo.
Intervention Type
Drug
Intervention Name(s)
Naproxen Sodium
Intervention Description
Dosed by weight (10mg/kg), twice daily, for 8 weeks
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Participants take placebo pills twice daily, for 8 weeks.
Primary Outcome Measure Information:
Title
Children's Yale-Brown Obsessive-Compulsive Scale, 2nd Edition (CY-BOCS-II)
Description
The CY-BOCS-II is a clinician-rated measure to assess obsessive-compulsive symptom severity. This results in two subscale total scores, Obsessions and Compulsion, each ranging from 0-25, with a higher score indicating more symptom severity. These subscale scores are summed to provide a total score, ranging from 0 to 50, that is used to measure overall OCD symptom severity.
Time Frame
Pre- to Post-8 week treatment
Title
Children's Yale-Brown Obsessive-Compulsive Scale, 1st Edition (CY-BOCS-I)
Description
The CY-BOCS-I is a clinician-rated measure to assess obsessive-compulsive symptom severity. This results in two subscale total scores, Obsessions and Compulsion, each ranging from 0-20, with a higher score indicating more symptom severity. These subscale scores are summed to provide a total score, ranging from 0 to 40, that is used to measure overall OCD symptom severity.
Time Frame
Pre- to Post-8 week treatment
Secondary Outcome Measure Information:
Title
Changes in C reactive protein pre- and post-treatment between groups
Description
C reactive protein (CRP, mg/L) will be obtained from pre- and post-blood draws and will be compared between groups.
Time Frame
Pre- to Post-8 week treatment
Title
Changes in erythrocyte sedimentation rate pre- and post-treatment between groups
Description
Erythrocyte sedimentation rate (ESR, mm/h) will be obtained from pre- and post-blood draws and will be compared between groups.
Time Frame
Pre- to Post-8 week treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Years
Maximum Age & Unit of Time
15 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 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. Exclusion Criteria: child who is acutely psychotic or suicidal 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 pre-existing liver, kidney, GI bleeding or clotting disorders (GFR <75 mL/min/1.73m2) history of ulcers in the digestive system history of restricted fluid intake, as this could exacerbate side effects concurrent antibiotic treatment or antibiotic treatment within one-week of baseline pregnant or becomes pregnant currently engaged in an intensive outpatient cognitive behavioral treatment program (more than weekly) 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) history of severe asthma or currently uncontrolled asthma
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sarah O'Dor, PhD
Phone
617-643-6688
Email
sodor@mgh.harvard.edu
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02114
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sarah O'Dor, PhD
Phone
617-726-8508
Email
PANDASclinic@partners.org
First Name & Middle Initial & Last Name & Degree
Saffron Homayoun
First Name & Middle Initial & Last Name & Degree
Kyle Williams, MD PhD

12. IPD Sharing Statement

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Trial of Naproxen Sodium for the Treatment of OCD in Children With PANDAS

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