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N-Acetylcysteine in Major Depressive Disorder Patients

Agumentation Effects of N-Acetylcysteine on signs of Major Depressive Disorder Patients treated with Antidepressants

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241112063684N1
Enrollment
60
Registered
2024-12-04
Start date
2024-12-15
Completion date
Unknown
Last updated
2025-01-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Signs of Major Depressive Disorder. Major depressive disorder, recurrent

Interventions

Intervention 1: Intervention group: After obtaining Informed Consent, they enter the study and in addition to receiving routine treatments for depression, for 8 weeks they are also treated with Naceth

Sponsors

Arak University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: Completion of Informed Consent by The legal guardian of Patient with Major Depression Disorder Fulfilling the Diagnostic Criteria for Major Depressive Disorder (First episode or recurrent episodes) Score of MADRS = 19 at the time of entering the study Treatment Stability of Patients for at least 2 weeks before Random Selection of Participants Effective use of Contraceptive Methods if women are of Reproductive age or Sexually active

Exclusion criteria

Exclusion criteria: Diagnosis of Bipolar Disorder I or II Primary Clinical Diagnosis of a Personality Disorder Received ECT within the last 6 Months Failure of 3 or more Steps of Adequate Antidepressant Medication Recent Using of more than 500 mg/d of N-acetyl cysteine and 200 µg/d of selenium and 500 IU/d of vitamin E Presence of Systemic Medical Disorder, Including Recent Gastrointestinal Ulcers, Pregnancy or Lactation, Epilepsy, Chronic Asthma Any Previous Allergic Skin Reaction or Anaphylaxis to N-Acetylcysteine

Design outcomes

Primary

MeasureTime frame
The number of patient whose score of Montgomery-Asberg Depression Scale (MADRS) is greater than 19. Timepoint: Examining the score of the Montgomery-Asberg Depression Scale (MADRS) before the start of the study and 8 weeks after treatment and 4 weeks after stopping treatment (12 weeks from the start of treatment). Method of measurement: Montgomery-Asberg Depression Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAli Mirbeygi

Arak University of Medical Sciences

a.mirbeigi@arakmu.ac.ir+98 86 3313 5075

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026