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Recruiting NCT05142735

NCT05142735 Effects of NAC on Symptoms of CHR Patients

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Clinical Trial Summary
NCT ID NCT05142735
Status Recruiting
Phase —
Sponsor Centre for Addiction and Mental Health
Condition Prodromal Schizophrenia
Study Type INTERVENTIONAL
Enrollment 90 participants
Start Date 2023-01-13
Primary Completion 2026-11-01

Eligibility & Interventions

Sex All sexes
Min Age 16 Years
Max Age 35 Years
Study Type INTERVENTIONAL
Interventions
N-AcetylcysteinePlacebo

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 90 participants in total. It began in 2023-01-13 with a primary completion date of 2026-11-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

Schizophrenia is a chronic debilitating psychotic disorder. Identifying persons with "clinical high-risk" (CHR) symptoms, which are like those of schizophrenia but less severe, and providing psychiatric care to these individuals has been shown to help prevent psychosis. Current medications used for CHR symptoms, however, are associated with substantial side effect burden. Therefore, practice guidelines do not recommend current medications as routine treatment for the CHR state, and there is a need to identify new treatments for this condition. Research suggests that abnormal brain oxidative stress may contribute to schizophrenia, offering a potential novel treatment target in the CHR state. Oxidative stress is an excess of free radicals, which are generated from normal metabolism and environmental exposures, and can damage cells. Antioxidants in the body normally neutralize free radicals. Antioxidant deficiency could result in excess oxidative stress that damages brain cells, leading to schizophrenia. Recent studies suggest that N-acetylcysteine (NAC), a precursor of the most abundant brain antioxidant, glutathione, may be a safe, well-tolerated treatment for schizophrenia. In light of this, NAC may also reduce symptoms and brain abnormalities in CHR patients.

Eligibility Criteria

Inclusion Criteria: 1. meeting Criteria of Psychosis-Risk Syndromes (COPS) criteria on the Structured Interview for Psychosis-Risk Syndromes (SIPS) 2. capacity to provide informed consent 3. if female, participant is not of child-bearing potential, defined as females who have undergone a sterilization procedure or have been post-menopausal for at least 1 year prior to screening OR participant is of child-bearing potential and agrees to use a medically approved method of birth control for the duration of the study Exclusion Criteria: 1. meeting criteria for any other DSM-5 diagnosis at the time of the study (except -personality disorder, nicotine use disorder, or other substance use disorder in full remission) 2. concomitant or past neurological condition 3. visual impairment which is not corrected to normal by prescription glasses history of reading disability 4. past antipsychotic treatment at a therapeutic dose 5. current treatment with a psychotropic medication except antidepressants on which the participants has been on a stable dose for at least 30 days. 6. pregnancy (as identified on self-report and/or rapid urine pregnancy test) or intent to become pregnant according to self-report 7. breastfeeding or plan to do so 8. history of kidney stones 9. current treatment with an antibiotic 10. current treatment with nitroglycerin 11. allergy to any ingredients in either the investigational product or placebo product

Contact & Investigator

Central Contact

Michael Kiang, MD, PhD

✉ michael.kiang@camh.ca

📞 416-535-8501

Principal Investigator

Michael Kiang, MD, PhD

PRINCIPAL INVESTIGATOR

Centre for Addiction and Mental Health

Frequently Asked Questions

Who can join the NCT05142735 clinical trial?

This trial is open to participants of all sexes, aged 16 Years or older, up to 35 Years, studying Prodromal Schizophrenia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05142735 currently recruiting?

Yes, NCT05142735 is actively recruiting participants. Contact the research team at michael.kiang@camh.ca for enrollment information.

Where is the NCT05142735 trial being conducted?

This trial is being conducted at Toronto, Canada.

Who is sponsoring the NCT05142735 clinical trial?

NCT05142735 is sponsored by Centre for Addiction and Mental Health. The principal investigator is Michael Kiang, MD, PhD at Centre for Addiction and Mental Health. The trial plans to enroll 90 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology