Signatures of N-Ac for Non-Suicidal Self-Injury in Adolescents
Primary Purpose
Self-Harm, Depression, Suicide
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
N-acetyl cysteine
Placebo oral tablet
Sponsored by
About this trial
This is an interventional treatment trial for Self-Harm
Eligibility Criteria
Inclusion Criteria:
- Current frequency of at least one NSSI episode in the past 2 months
- ≥ 5 past episodes of NSSI with significant tissue damage (e.g. scars present)
- Psychotropic medications are dose-stable for 1 month
- Ability to understand study procedures and to comply with them for the entire length of the study
Exclusion Criteria:
- Any MRI contraindications (e.g. metal plates, claustrophobia, braces, implanted devices)
- Any current serious medical illness as defined by medical history
- Current Substance Use Disorder (except Tobacco Use Disorder)
- Primary psychotic disorder (e.g. schizophrenia, schizoaffective disorder, schizophreniform disorder)
- Neurodevelopmental disorder such as mental retardation or autism
- Changes in psychotropic medications in past 1 month
- Taken NAC or glutathione on a regular basis in the past 6 months
- Currently pregnant, planning to become pregnant, currently breastfeeding, or unwillingness to use contraception throughout the study.
- Allergy/sensitivity to N-acetylcysteine.
- Inability or unwillingness of individual or legal guardian/representative to give written informed consent.
Sites / Locations
- University of Minnesota
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Experimental
Placebo Comparator
Arm Label
Low-Dose NAC
High-Dose NAC
Placebo
Arm Description
3600 NAC mg/day
5400 NAC mg/day
Placebo
Outcomes
Primary Outcome Measures
Percent Increase in Glutathione (GSH) Concentrations in the ACC
increase in glutathione (GSH) concentrations in the anterior cingulate cortex (ACC) as measured by magnetic resonance spectroscopy (MRS)
Secondary Outcome Measures
Change in GSH Reduced-to-oxidized Ratio
Percent increase in reduced-to-oxidized ratio of glutathione (GSH) in the blood compared to baseline
Change in Glutamate Concentrations
Percent decrease in the concentrations of glutamate (GLU) in the anterior cingulate cortex (ACC) measured by MRS
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT04005053
Brief Title
Signatures of N-Ac for Non-Suicidal Self-Injury in Adolescents
Official Title
Identifying Biological Signatures of N-Acetylcysteine for Non-Suicidal Self-Injury in Adolescents and Young Adults
Study Type
Interventional
2. Study Status
Record Verification Date
July 2023
Overall Recruitment Status
Completed
Study Start Date
August 1, 2019 (Actual)
Primary Completion Date
May 8, 2022 (Actual)
Study Completion Date
October 1, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Minnesota
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
To measure NAC-induced changes to concentrations of glutathione (GSH) in the anterior cingulate cortex (ACC) as measured by magnetic resonance spectroscopy (MRS) in 36 adolescents and young adults with NSSI (12 in each group: high, low, and placebo).
Detailed Description
This study is a double-blind, placebo controlled, 4-week course of two-tiered N-acetylcysteine (NAC) dosing focused on identifying the optimal dose to achieve meaningful change in measurable biomarkers (glutathione and glutamate).
This design will allow us to confirm acute biological changes, select the optimal dose for achieving biological effects, and examine dose/concentration-response relationships with respect to biological markers and pharmacokinetics.
Brief schedule of activities: Subjects will be recruited through community and clinical settings and screened over the phone. There will be a total of 4 in-person visits and two sets of on-line study activities.
Eligible participants will be assigned to one of 3 groups (double-blinded): a low-dose NAC group (3600 mg/day), a high-dose NAC group (5400mg/day), and placebo (PBO). The study intervention period is 4 weeks. Total participation is up to 8 weeks, depending on the length of time between Day 0 and Day 1.
The investigators will recruit 36 adolescents and young adults aged 16-24 years. There will be 12 participants in each group (PBO, 3600mg/day, 5400mg/day). The investigators will use a minimization procedure to ensure that the participants in these 3 groups will have similar age, clinical severity and medication status.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Self-Harm, Depression, Suicide
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
44 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Low-Dose NAC
Arm Type
Experimental
Arm Description
3600 NAC mg/day
Arm Title
High-Dose NAC
Arm Type
Experimental
Arm Description
5400 NAC mg/day
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Intervention Type
Drug
Intervention Name(s)
N-acetyl cysteine
Other Intervention Name(s)
N-acetylcysteine
Intervention Description
3600 or 5400 mg/day N-acetyl cysteine
Intervention Type
Drug
Intervention Name(s)
Placebo oral tablet
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Percent Increase in Glutathione (GSH) Concentrations in the ACC
Description
increase in glutathione (GSH) concentrations in the anterior cingulate cortex (ACC) as measured by magnetic resonance spectroscopy (MRS)
Time Frame
28 days
Secondary Outcome Measure Information:
Title
Change in GSH Reduced-to-oxidized Ratio
Description
Percent increase in reduced-to-oxidized ratio of glutathione (GSH) in the blood compared to baseline
Time Frame
28 days
Title
Change in Glutamate Concentrations
Description
Percent decrease in the concentrations of glutamate (GLU) in the anterior cingulate cortex (ACC) measured by MRS
Time Frame
28 days
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
24 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Current frequency of at least one NSSI episode in the past 2 months
≥ 5 past episodes of NSSI with significant tissue damage (e.g. scars present)
Psychotropic medications are dose-stable for 1 month
Ability to understand study procedures and to comply with them for the entire length of the study
Exclusion Criteria:
Any MRI contraindications (e.g. metal plates, claustrophobia, braces, implanted devices)
Any current serious medical illness as defined by medical history
Current Substance Use Disorder (except Tobacco Use Disorder)
Primary psychotic disorder (e.g. schizophrenia, schizoaffective disorder, schizophreniform disorder)
Neurodevelopmental disorder such as mental retardation or autism
Changes in psychotropic medications in past 1 month
Taken NAC or glutathione on a regular basis in the past 6 months
Currently pregnant, planning to become pregnant, currently breastfeeding, or unwillingness to use contraception throughout the study.
Allergy/sensitivity to N-acetylcysteine.
Inability or unwillingness of individual or legal guardian/representative to give written informed consent.
Facility Information:
Facility Name
University of Minnesota
City
Minneapolis
State/Province
Minnesota
ZIP/Postal Code
55455
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34036177
Citation
Sahasrabudhe SA, Silamongkol T, Park YW, Colette A, Eberly LE, Klimes-Dougan B, Coles LD, Cloyd JC, Oz G, Mueller BA, Kartha RV, Cullen KR. Identifying Biological Signatures of N-Acetylcysteine for Non-Suicidal Self-Injury in Adolescents and Young Adults. J Psychiatr Brain Sci. 2021;6:e210007. doi: 10.20900/jpbs.20210007. Epub 2021 Apr 29.
Results Reference
derived
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Signatures of N-Ac for Non-Suicidal Self-Injury in Adolescents
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