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Not yet recruiting NCT04381897

Use of N-Acetylcysteine in the Treatment of Repetitive and Self-Injurious Behaviors in Cornelia de Lange Syndrome

Phase II Interventional Cornelia de Lange Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: N-acetyl cysteine, Placebo.
Who it may be relevant to
Registry conditions: Cornelia de Lange Syndrome. Basic parameters: 13 years — 35 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Use of N-Acetylcysteine (NAC) in the Treatment of Repetitive Behaviors (RB) and Self-Injurious Behaviors (SIB) in Cornelia de Lange Syndrome: A Randomized Double-Blind Placebo-Controlled Pilot Study

Overview

This research project is a randomized cross-over pilot trial which aims to test the efficacy of N-acetylcysteine (NAC) for the treatment of Repetitive Behaviors (RB) and self-injurious behavior (SIB) in patients with Cornelia de Lange Syndrome (CdLs). NAC is a known anti-oxidative stress and neuroprotective agent, which has been shown to decrease the occurrence of SIB such as skin picking. NAC has also shown partial response in trials for compulsive behaviors in Obsessive Compulsive Disorder (OCD) and related disorders in autism. Cornelia de Lange syndrome (CdLS) is a genetic disorder with autistic features, including RBs and SIB. In this randomized clinical trial, participants with CdLS will be blindly assigned one of two possible treatment arms: 1) placebo (8 weeks) and NAC (8 weeks); or 2) NAC (8 weeks) and placebo (8 weeks), with an intermediate 2-week washout period.

Detailed description

Cornelia de Lange syndrome (CdLS) is a genetic condition caused by mutations in cohesin-related genes, mostly notably NIPBL. The CdLS phenotype includes physical features such as typical facies, limb abnormalities, short stature, and hirsutism as well developmental and behavioral manifestations such as intellectual disability, communication deficits, autistic traits and repetitive/self-injurious behaviors (RBs/SIB).

Behavioral challenges such as RBs/SIB pose a significant obstacle to quality of life to individuals with CdLS and families. In CdLS, disruption of developmental systems can impact neuronal and brain development, and impact GABAergic inhibitory interneuron formation, leading to RBs/SIB. Given the potential for dysregulated excitatory glutamatergic output in CdLS, neuronal oxidative stress may play a role in these maladaptive behaviors. NAC replenishes Central Nervous System (CNS) glutathione, a potent antioxidant and may ameliorate RBs/SIB. NAC has been shown to decrease maladaptive behaviors in autism and grooming disorders such as excoriation disorder (skin picking).

An 18-week cross-over trial is proposed to decrease RBs/SIB comprising two 8-week double-blinded active or placebo treatment with a 2-week wash out period in between. A cross-over design will afford for higher efficiency in sample size for similar power. Dosage will be titrated weekly starting at 600 mg daily and then increased by 600 mg every week to a target dose of 1800 mg per day. Participants will be recruited through CdLS Foundation.

Based on a mechanism for regulation glutamate transmission homeostasis in the central nervous system, the use of NAC may be particularly pertinent to individuals with CdLS. It is known that in CdLS genetic networks that impact on limb formation overlap significantly with developmental systems that impact neuronal and brain development, in particular GABAergic inhibitory interneuron formation. Given a dysregulated excitatory glutamatergic mechanism due to interneuron deficits, which can then lead to neuronal oxidative stress and programmed cell death, NAC may act as a key homeostatic regulator to prevent glutamate overactivity and neuronal damage in CdLS.

Interventions

  • Drug N-acetyl cysteine
    Oral solution for N-acetyl cysteine is prepared in syringes and provided to the participants along with instructions on how to administer them.
  • Other Placebo
    NAC Placebo-matching solution is prepared in syringes and provided to the participants along with instructions on how to administer them.

Primary outcome measures

  • Change in Children's Yale-Brown Obsessive Compulsive Scale Modified for Pervasive Developmental Disorders (CYBOCS-PDD) repetitive behaviors measure score [Time frame: Baseline, week 2, week 4, week 6, week 8, week 10, week 12, week 14, week 16, week 18]
  • Change in Aberrant Behavior Checklist (ABC) irritability self-injurious behaviors items score [Time frame: Baseline, week 2, week 4, week 6, week 8, week 10, week 12, week 14, week 16, week 18]
Secondary outcome measures (8)
  • Change in Aberrant Behavior Checklist (ABC) irritability non-injurious behaviors items score [Time frame: Baseline, week 2, week 4, week 6, week 8, week 10, week 12, week 14, week 16, week 18]
  • Change in total score of Parenting Stress Index/Short Form (PSI/SF) [Time frame: Baseline, week 8, week 10, week 18]
  • Change in Burden Scale for Family Caregivers score [Time frame: Baseline, week 8, week 10, week 18]
  • Change in Sensory Profile score [Time frame: Baseline, week 8, week 10, week 18]
  • Change in Childhood Autism Rating Scale (CARS2) score [Time frame: Baseline, week 8, week 10, week 18]
  • Change in Vineland adaptive Behavior Scale (VABS) score [Time frame: Baseline, week 8, week 10, week 18]
  • Change in Clinical Global Impression - Severity of Illness (CGI-S) score [Time frame: Baseline, week 8, week 10, week 18]
  • Change in Side Effects Survey [Time frame: Baseline, week 2, week 4, week 6, week 8, week 10, week 12, week 14, week 16, week 18]

Eligibility criteria

Inclusion criteria

  • Ages 13 to 35 years
  • A diagnosis of CdLS as determined by a physician during routine care meeting the major and minor criteria from CdLS guidelines
  • Threshold criteria for the presence of RB/SIB as reported on initial screening Children's Yale-Brown Obsessive Compulsive Scale Modified for Pervasive Developmental Disorders (CYBOCS-PDD) > 6 OR Aberrant Behavior Checklist (ABC) stereotypy subscale > 7)
  • Being able to attend 4 visits over the course of 18 weeks at the Johns Hopkins Hospital
  • No acute safety concerns or need for hospitalization due to psychotic, manic or depressive episode
  • Not currently pregnant or lactating/breastfeeding. Whether a participant is pregnant or not will be determined by the participant/caregiver report based on date last menses. If there is any suspicion of pregnancy, the PI will confer with the family to obtain testing through the primary care provider.

Exclusion criteria

  • Allergy to NAC
  • Allergy to Quinine
  • Contraindication to NAC (organ transplant; untreated or symptomatic gastric condition)
  • Need for another medication with which NAC is contraindicated (antibiotics)

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Crossover
Masking
Triple blind
Primary purpose
Treatment

Study locations

United States · 1 center
  • Johns Hopkins University School of Medicine — Baltimore

Publications

  • Hardan AY, Fung LK, Libove RA, Obukhanych TV, Nair S, Herzenberg LA, Frazier TW, Tirouvanziam R. A randomized controlled pilot trial of oral N-acetylcysteine in children with autism. Biol Psychiatry. 2012 Jun 1;71(11):956-61. doi: 10.1016/j.biopsych.2012.01.014. Epub 2012 Feb 18. PMID 22342106

Identifiers

NCT: NCT04381897 · IRB00153778

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗