The Effect of N- Acetylcysteine on Inflammatory and Oxidative Stress Biomarkers (nac)
Bipolar Disorder
About this trial
This is an interventional treatment trial for Bipolar Disorder focused on measuring Tobacco use disorder and bipolar disorders, N-acetylcysteine, Oxidative stress, inflammation
Eligibility Criteria
Inclusion Criteria:
- To be included in this study participants must be motivated smokers to stop tobacco use
- Age greater than or equal to 18 and less than 65 years
- Both sexes
- All races
- Capacity to consent to the study and carefully follow the guidelines and procedures and sign the term of free and informed consent .
- Will be included with comorbid bipolar, depressive and anxiety disorder with tobacco use by more than 20 cigarettes per day, and a control group without these mood disorders and without tobacco use disorder.
Exclusion Criteria:
We excluded any subjects with: abnormal blood values on the following laboratory tests: *hemogram, aspartate transaminase (AST), alanine transaminase (ALT), urea and creatinine
- other actual and life-time axis-I diagnoses (including schizophrenia, psycho-organic syndromes, delirium, dementia, amnestic, and other cognitive disorders)
- medical illness, including HIV and hepatitis B and C, (auto)immune disorders
- immune modulatory drugs, e.g. glucocorticoids and use of antioxidants.
- These situations can affect an inflammatory and / or immune process.
Sites / Locations
- State University of Londrina
Arms of the Study
Arm 1
Arm 2
Active Comparator
Placebo Comparator
NAC ( baseline )and 12 week
placebo ( baseline ) and 12 week
subjects with tobacco use disorder (TUD) and bipolar disorders who will receive N-acetyl-cysteine (NAC) or placebo at baseline for a period of 12 weeks The participants with TUD (n=72) and they will receive a 1800mg per day of NAC or matching placebo . There will be asses laboratory examinations for inflammatory and oxidative stress biomarkers at baseline and at 12 week
subjects with tobacco use disorders (TUD and bipolar disorders who will receive N-acetyl-cysteine (NAC) or placebo for a period of 12 weeks. The participants with TUD and bipolar disorders (n=72) and they will receive a 1800mg per day of NAC or matching placebo . There will be assessed laboratory examinations for inflammatory and oxidative stress biomarkers at baseline and at 12 week