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Search / Trial NCT01172275

N-acetylcysteine (NAC) for Pediatric Obsessive-Compulsive Disorder

Launched by YALE UNIVERSITY · Jul 28, 2010

Trial Information

Current as of June 20, 2025

Completed

Keywords

Obsessive Compulsive Disorder Ocd

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Children aged 8-17 years.
  • Primary diagnosis of OCD.
  • Duration of OCD greater than 6 months.
  • Significant Current OCD symptoms: Current CY-BOCS score \> or = 16.
  • Exclusion Criteria:
  • Comorbid bipolar disorder, psychotic disorder, substance use disorder, developmental disorder or mental retardation (IQ\<70).
  • Recent change (less than 4 weeks) in medications that have potential effects on OCD severity (such as Selective Serotonin Reuptake Inhibitors, clomipramine, naltrexone, lithium, psychostimulants, anxiolytics, or antipsychotics). Medication change is defined to include either dose changes or medication discontinuation.
  • Recent change in behavioral treatment for OCD or comorbid conditions within the last 4 weeks or initiation of behavioral therapy for tics within the last 12 weeks.
  • Asthma requiring medication use within the last 3 months (case reports have linked intravenous NAC administration with asthma exacerbation)
  • Known hypersensitivity or previous anaphylactoid reaction to acetylcysteine or any components in its preparation.
  • Positive pregnancy test or drug screening test.
  • Previous use of N-acetylcysteine (dose greater than 600mg for more than 2 weeks).
  • Previous history or suspicion of cystinuria because of a possibility of forming kidney stones.

About Yale University

Yale University, a prestigious Ivy League institution located in New Haven, Connecticut, is renowned for its commitment to advancing medical research and clinical innovation. With a rich history of academic excellence and a robust infrastructure for scientific inquiry, Yale serves as a leading sponsor for clinical trials aimed at improving patient care and developing new therapeutic approaches. The university's multidisciplinary teams of researchers and clinicians collaborate to conduct rigorous and ethical studies, leveraging cutting-edge technologies and methodologies to address critical health challenges. Through its dedication to fostering an environment of inquiry and discovery, Yale University plays a pivotal role in translating research findings into clinical practice, ultimately enhancing health outcomes for diverse populations.

Locations

New Haven, Connecticut, United States

Patients applied

0 patients applied

Trial Officials

Michael H. Bloch, MD, MS

Principal Investigator

Yale University

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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