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N/A Completed N=35 Treatment

Efficacy Study of Korean Red Ginseng to Treat Depression

Source: ClinicalTrials.gov NCT01496248 ↗
Enrolled (actual)
35
Serious AEs
0.0%
Results posted
Oct 2014
Primary outcomePrimary: Depression Residual Symptom Scale — 21.8 units on a scale — p=<0.05

Summary

The purpose of this study is to determine whether Korean Red Ginseng are effective in the treatment of the residual symptoms of depression as an adjuvant treatment.

Outcome Measures

OutcomeResultp-value
PRIMARY
Depression Residual Symptom Scale
17.5 <0.05 sig
SECONDARY
Visual Analogue Scale
28.0 <0.05 sig
SECONDARY
Montgomery Asberg Depression Rating Scale
4.4 <0.05 sig
SECONDARY
Clinical Global Index
2.4 <0.05 sig

Eligibility Criteria

Inclusion Criteria

  • Outpatients who met Diagnostic and Statistical Manual of Mental Disorders (DSM-IV) criteria for major depressive disorder.
  • Those who are in remission, which is defined as a MADRS score 8 on two consecutive visits at a 4-week interval.
  • Their primary psychiatric clinician determined that they would benefit from an adjuvant treatment of Korean red ginseng for residual symptoms.

Exclusion Criteria

  • Those who have a history of substance abuse or dependence within 1 month.
  • Those who have clinically significant abnormal laboratory values or any other abnormal baseline laboratory findings considered by psychiatrists to be indicative of conditions that might affect the study results.
  • Those who have a past history of hypersensitivity or intolerance to Korean red ginseng.
  • Those who participated in clinical trials within 1 month before entering the study entry.
  • Those who are pregnant or are breast feeding.
  • Those who have a immediate risk of harming self or others or history of suicide attempts in the year before the screening precluded inclusion in the study.
  • The patients unable/unlikely to comprehend/follow the protocol.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01496248). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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