N-Acetyl Cysteine Supplementation in Therapy Refractory Major Depressive Disorders

Sponsor

Tianjin Anding Hospital (Other)

Overall Status

Recruiting

CT.gov ID

NCT02972398

Collaborator

(none)

200

Enrollment

Location

Arms

Anticipated Duration (Months)

2.4

Patients Per Site Per Month

Study Details

Study Description

Brief Summary

The aim of this study is to evaluate the efficacy of N-acetylcysteine (NAC) add-on to antidepressant medication in treating patients who do not relieve during standard antidepressant treatment for 6 weeks at least. Meanwhile, secondary outcomes will include changes in some biomarkers and on specifically local brain activity (functional Magnetic Resonance Imaging, fMRI) and white matter integrity (Diffusion Tensor Imaging, DTI). The hypothesis of this study is that NAC has positive effects on refractory major depressive disorder patients with increased inflammatory activity.

Condition or Disease	Intervention/Treatment	Phase
Major Depressive Disorders	Drug: N-acetylcysteine Drug: placebo comparator of N-acetylcysteine	N/A

Detailed Description

It's a double-blind randomised placebo controlled antidepressant augmentation study with 12-week treatment and 8-week follow up. Its purpose is to investigate antidepressant efficacy and safety of NAC in patients with treatment resistant depression (TRD) defined as insufficient response to 1 or more antidepressants given for at least 6 weeks and in an adequate dose, displaying increased peripheral inflammatory activity and moderate to severe depression. Apart from studying the effects of NAC on depression severity, the secondary outcomes are to examine a range of biomarkers related to potentially important underlying mechanisms such as oxidative stress and inflammatory activity and to evaluate the effects on brain functioning (fMRI) and on white matter integrity (DTI). Scale assessments are performed in the week preceding initiation of treatment, during the treatment period, at the end of the treatment period and at 8-week follow up. Neuro-imaging is performed before the treatment starts and in week 12, before the study medication is terminated. Collection of blood and morning urine only takes place at three time points, in the week preceding initiation of treatment, closely before tapering off the study medication and at the end of 8-week follow up. This study is hoped to show that NAC perform positive effects on those aspects mentioned above.

Study Design

Study Type:

Interventional

Anticipated Enrollment :

200 participants

Allocation:

Randomized

Intervention Model:

Parallel Assignment

Masking:

Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Primary Purpose:

Treatment

Official Title:

N-Acetyl Cysteine add-on to Antidepressant Medication in Therapy Refractory Major Depressive Disorder Patients With Increased Inflammatory Activity

Actual Study Start Date :

Sep 1, 2015

Anticipated Primary Completion Date :

Jul 1, 2022

Anticipated Study Completion Date :

Sep 1, 2022

Arms and Interventions

Arm	Intervention/Treatment
Experimental: NAC group Participants of "NAC group" receive 1000 mg NAC twice daily for 12 weeks as add-on to either a selective serotonin reuptake inhibitor (SSRI) or a serotonin and noradrenalin reuptake inhibitor (SNRI)	Drug: N-acetylcysteine Participants of interventional group receive 1000mg N-acetylcysteine twice daily for 12 weeks. Other Names: YiWeiShi
Placebo Comparator: Placebo group Participants of "Placebo group" receive placebo matched with NAC twice daily for 12 weeks as add-on to either a selective serotonin reuptake inhibitor (SSRI) or a serotonin and noradrenalin reuptake inhibitor (SNRI)	Drug: placebo comparator of N-acetylcysteine Participants of placebo group receive placebo comparator matching with N-acetylcysteine twice daily for 12 weeks.

Arm

Intervention/Treatment

Experimental: NAC group

Participants of "NAC group" receive 1000 mg NAC twice daily for 12 weeks as add-on to either a selective serotonin reuptake inhibitor (SSRI) or a serotonin and noradrenalin reuptake inhibitor (SNRI)

Drug: N-acetylcysteine

Participants of interventional group receive 1000mg N-acetylcysteine twice daily for 12 weeks.

Other Names:

YiWeiShi

Placebo Comparator: Placebo group

Participants of "Placebo group" receive placebo matched with NAC twice daily for 12 weeks as add-on to either a selective serotonin reuptake inhibitor (SSRI) or a serotonin and noradrenalin reuptake inhibitor (SNRI)

Drug: placebo comparator of N-acetylcysteine

Participants of placebo group receive placebo comparator matching with N-acetylcysteine twice daily for 12 weeks.

Outcome Measures

Primary Outcome Measures

The change from baseline Hamilton Depression Rating Scale (HAMD)-17 items at week2,4,6,8,10,and 12. [baseline, Week 2,4,6,8,10, and 12]
The main objective is to investigate whether daily oral NAC administration in addition to regular treatment with an antidepressant will alleviate the severity of MDD symptoms as measured with the HAMD-17 after 12 weeks of treatment compared to placebo addition, and we also look at other time points, such as week 2,4,6,8,and 10.

Secondary Outcome Measures

The change from baseline HAMD-17 items at week14,16,18,and 20. [baseline, Week 14,16,18,and 20.]
We also look at whether daily oral NAC treatment will still have measurable effects on HAMD-17 score at 8 weeks follow-up after discontinuation of NAC treatment.
The effects of augmentation treatment with NAC on scores in Beck Anxiety Inventory (BAI) [baseline, Week 4,8,12,16,and 20.]
The effects of augmentation treatment with NAC on scores in Inventory of Depressive Symptoms-Self-Rated (IDS-SR) [baseline, Week 4,8,12,16,and 20.]
The effects of augmentation treatment with NAC on scores in WHO Disability Assessment Schedule Ⅱ (WHODAS-Ⅱ) [baseline, Week 4,8,12,16,and 20.]
The effects of augmentation treatment with NAC on scores in Montreal Cognitive Assessment (MoCA) [baseline, Week 4,8,12,16,and 20.]
The effects of augmentation treatment with NAC on local brain activity (fMRI and DTI) [baseline, the end of week 12.]
The effects of augmentation treatment with NAC on a range of biomarkers representing the alleged underlying pathophysiological mechanisms [baseline, the end of the week 12 and 20]
biomarkers associated with inflammation, oxidative stress, and neurogenesis in sample of serum and urine.
Assessments the side effects measured with Checklist of 52 Somatic Items (CSI) [baseline, Week 4,8,12,16,and 20.]

Eligibility Criteria

Criteria

Ages Eligible for Study:

18 Years to 65 Years

Sexes Eligible for Study:

All

Accepts Healthy Volunteers:

Inclusion Criteria:

a current episode of MDD diagnosed according to Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV-TR) diagnosed with SCID
an age between 18 and 65 years
a total score of HAMD-17 ≥ 17
a CRP level between 0.85 and 10 mg/L (The CRP range is based on literature values for mild to moderate chronic inflammation, while values > 10 mg/L point at acute inflammation. A pilot study at the Tianjin Hospital (n=62) indicated that approximately one third of all patients with MDD will have CRP values within this range). insufficient response to 1 or more antidepressants given for at least 6 weeks and in an adequate dose during the current episode
stable dose of the current antidepressant drug for at least 2 weeks prior to initiation of the study
Patients are allowed to use benzodiazepines (BZD) to relieve anxiety during the first phase of antidepressant treatment (Anding Hospital protocol). Benzodiazepines may also be prescribed because of sleeping problems during the trial. BZD use will be recorded at all assessments during the trial and after follow-up.
Patients are compliant with treatment according to the judgement of the treating clinician.
Female subjects will be eligible to participate in the study if they are of non-childbearing potential or of child-bearing potential and willing to practice appropriate birth control methods during the study. Clinical patients always get a pregnancy test before start of treatment.
Participant or guardian has to sign informed consent. The patients' guardians will sign the informed consent on behalf of the participants when the capacity of participants to consent is compromised.

Exclusion Criteria:

A history of manic episode
Use of mood stabilizer
Use of antipsychotic medication with more than half of the maximum dosage suggested in the instruction
History of substance abuse or dependence
An allergic reaction to NAC or any component of the preparation
Severe somatic diseases that might interfere with regular antidepressant treatment including conditions such as kidney and liver failure, uncontrolled hypertension, cardiovascular, cerebrovascular and pulmonary disease, thyroid disease, diabetes, epilepsy and asthma.
Use of anti-inflammatory medication for longer than 7 days in the last two months preceding the trial
Use of immunosuppressive medication such as oral steroid hormones
History of chronic infection, such as Tuberculosis, AIDS, hepatitis
CRP value > 10 mg/L
Women in pregnancy or lactation period