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Completed

NCT Number: NCT00446719

Safety and Antidepressant Effects of Rellidep in Major Depressive Disorder

The investigators hypothesize that Rellidep will be effective in improving the symptoms of major depression. The available evidence strongly suggests that Rellidep contains a mood altering ingredient or ingredients. This open-label, non-randomized study sets out to validate its potential antidepressant activity.The study will include secondary aims of evaluating the effect of Rellidep on reducing symptoms of anxiety, a common symptom associated symptom of depression and improving quality of life.

About twenty-five patients with major depressive disorder will be assigned to open-label Rellidep (2000 mg/day) for a period of 8 weeks. All patients will be assessed by various measures of global improvement, depression, quality of life, sexual experience, anxiety and measures of side effects as well as standard laboratory tests.

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Key information

Age range

18 year–64 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Mount Sinai Hospital

Toronto, Ontario, M5G 1X5, Canada

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Signed written informed consent obtained.
  • Males/Females 20-65 years of age who require a new or a new change in their medication treatment for diagnosed major depression.
  • A clinical diagnosis fulfilling DSM-IVTR criteria for Major Depressive Disorder, single episode or recurrent.
  • 17-Item Hamilton Depression Rating Scale (HAMD 17-item) total score at baseline of 18 or higher

Exclusion criteria

  • Clinical diagnosis of depression other than DSM-IVTR Major Depressive Disorder (single episode/recurrent, e.g. chronic depression and/or refractory depression are excluded).
  • Judged to be at significant risk for suicide or having a history suggesting significant current potential for self harm.
  • Antidepressant medication (other than the index antidepressant).
  • Women who are pregnant or breast-feeding or intending to become pregnant in the next 12 months.
  • Clinically significant organ system diseases, e.g. cardiovascular, hepatic, renal, endocrine, gastrointestinal, metabolic, or other systemic diseases.
  • Course of electroconvulsive therapy (ECT) during the observational period.
  • Suffer from a major neurological condition (i.e., Parkinson's disease, Huntington's disease), cerebrovascular disease (i.e., stroke), metabolic conditions (i.e., Vitamin B12 deficiency), autoimmune conditions (i.e., systematic lupus erythematosus), viral or other infections (i.e., hepatitis, mononucleosis, human immunodeficiency), and cancer.
  • Current diagnosis of Schizophrenia or other psychotic disorders (including Schizophreniform Disorder, Schizoaffective Disorder, Delusional Disorder, brief psychotic disorders, psychotic disorder due to general medical condition, substance induced psychotic, psychotic disorder not otherwise specified) as defined in the DSM-IV.
  • (Sub) clinical hypo/hyper thyroidism (e.g. elevated TSH).

Treatment and study plan

Rellidep

Drug

2000 mg P.O. daily for 8 weeks

Primary outcomes

  1. 50% improvement on Hamilton Depression Rating Scale-17 at 8 weeks

    Time frame: 8 weeks

Secondary outcomes

  1. Clinical Global Impression-Severity and Improvement

    Time frame: 8 weeks

  2. Montgomery Asberg Depression Rating Scale (MADRS) at 8 weeks

    Time frame: 8 weeks

  3. Medical Outcomes Study Short-Form 36 (SF-36)at 8 weeks

    Time frame: 8 weeks

  4. Beck Depression Inventory Scale (BDI) a t 8 weeks

    Time frame: 8 weeks

  5. Hamilton rating scale for Anxiety (HAM-A)at 8 weeks

    Time frame: 8 weeks

  6. UKU

    Time frame: 8 weeks

Sponsors and collaborators

Lead sponsor

Mount Sinai Hospital, Canada

Other

Registry information

Official study title

An Open-Label Pilot Study Evaluating the Safety and Antidepressant Effects of Rellidep (BI= Biological Isolate) in Major Depressive Disorder

Important dates

Study start
2007
Primary completion
2008
Study completion
2008
First posted
Mar 13, 2007
Registry last updated
Jan 5, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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