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American Ginseng Treatment for Multiple Sclerosis Related Fatigue

Primary Purpose

Multiple Sclerosis

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
American ginseng extract HT-1001
placebo
Sponsored by
Oregon Health and Science University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Multiple Sclerosis focused on measuring Multiple sclerosis, fatigue, ginseng

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • MS as diagnosed by the McDonald criteria
  • Complaint of fatigue that has been persistent for at least 2 months
  • FSS score of 4 or greater;
  • Age 18-70.

Exclusion Criteria:

  • Use of ginseng or stimulants in the prior 6 weeks
  • Acute treatment with glucocorticoids in the prior 6 weeks
  • BDI >31
  • Significant MS exacerbation in prior 30 days
  • Diabetes
  • Uncontrolled hypertension
  • Other serious medical disease, pregnancy or breastfeeding
  • Breast disease
  • Abnormal bleeding or clotting disorder
  • Current use of warfarin, albendazole, nifedipine, digoxin, bumetadine, selegiline, isocarboxazid, or phenelzine
  • Current use of lasix for poorly controlled hypertension or congestive heart failure
  • Current drug or alcohol abuse; inability to complete the self report forms

Sites / Locations

  • Oregon Health & Science University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

1

2

Arm Description

Period 1 with Ginseng therapy intervention; Washout Period with no drug; Period 2 with placebo

Period 1 with placebo; Washout period with no drug; Period 2 with ginseng therapy intervention

Outcomes

Primary Outcome Measures

Fatigue Severity Scale
The Fatigue Severity Scale (FSS)is a self-administered instrument that includes 9 items rated on a 7-point scale, measuring fatigue severity. The subject is asked to score each statement, based on how the statement applied to them over the preceding week. The fatigue severity score is the average of the scores on the 9 questions; scores range from 1-7, with lower scores indicating less fatigue.

Secondary Outcome Measures

Modified Fatigue Impact Scale
21 item scale, score range 0-84, lower scores indicate less fatigue
Realtime Digital Fatigue Score
fatigue scored on 0-10 scale with higher scores indicating more fatigue

Full Information

First Posted
September 16, 2008
Last Updated
January 20, 2012
Sponsor
Oregon Health and Science University
Collaborators
National Multiple Sclerosis Society
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1. Study Identification

Unique Protocol Identification Number
NCT00754832
Brief Title
American Ginseng Treatment for Multiple Sclerosis Related Fatigue
Official Title
A Double-blinded, Placebo-controlled Crossover Pilot Study of American Ginseng Treatment for Multiple Sclerosis Related Fatigue
Study Type
Interventional

2. Study Status

Record Verification Date
January 2012
Overall Recruitment Status
Completed
Study Start Date
September 2005 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
March 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oregon Health and Science University
Collaborators
National Multiple Sclerosis Society

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This research project will determine the safety and tolerability of ginseng in subjects with MS and will gather preliminary data on the efficacy of ginseng vs placebo for the treatment of MS fatigue.
Detailed Description
Fatigue is a major cause of disability in MS and is associated with a reduced quality of life. Treatment options for MS fatigue include central nervous system stimulants and amantadine. These medications are of limited efficacy, are often poorly tolerated, and can be expensive. Ginseng may represent a novel approach to treating MS fatigue. Ginseng has been tested in clinical trials for its ability to improve mental alertness and fatigue. However, there have been no published clinical trials addressing the effects of ginseng in subjects with MS, even though many people with MS use ginseng and report deriving benefit from it. This double-blinded, placebo controlled crossover pilot study will determine the safety and tolerability of ginseng in subjects with MS and will gather preliminary data on the efficacy of ginseng vs. placebo for the treatment of MS fatigue. Additionally, the project will collect information on the impact of ginseng on cognition, stress, actigraphy, salivary cortisol, differential cytokine response, and quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis
Keywords
Multiple sclerosis, fatigue, ginseng

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
56 (Actual)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Period 1 with Ginseng therapy intervention; Washout Period with no drug; Period 2 with placebo
Arm Title
2
Arm Type
Experimental
Arm Description
Period 1 with placebo; Washout period with no drug; Period 2 with ginseng therapy intervention
Intervention Type
Drug
Intervention Name(s)
American ginseng extract HT-1001
Intervention Description
Ginseng HT-1001 was dosed at 100 mg orally per day initially, increased after one week to 200 mg per day, then further increased the next week to 400 mg per day as tolerated. Subjects were then maintained on 400 mg per day or the maximum tolerated dose for the remainder of the 6 week treatment period.
Intervention Type
Drug
Intervention Name(s)
placebo
Other Intervention Name(s)
placebo (matched capsules to ginseng drug)
Intervention Description
Placebo capsules were identical to the study drug and were dose escalated to match the study drug. Subjects were maintained on placebo capsules for the remainder of the 6 week treatment period.
Primary Outcome Measure Information:
Title
Fatigue Severity Scale
Description
The Fatigue Severity Scale (FSS)is a self-administered instrument that includes 9 items rated on a 7-point scale, measuring fatigue severity. The subject is asked to score each statement, based on how the statement applied to them over the preceding week. The fatigue severity score is the average of the scores on the 9 questions; scores range from 1-7, with lower scores indicating less fatigue.
Time Frame
after 6 weeks of intervention
Secondary Outcome Measure Information:
Title
Modified Fatigue Impact Scale
Description
21 item scale, score range 0-84, lower scores indicate less fatigue
Time Frame
6 weeks of intervention
Title
Realtime Digital Fatigue Score
Description
fatigue scored on 0-10 scale with higher scores indicating more fatigue
Time Frame
6 weeks of intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: MS as diagnosed by the McDonald criteria Complaint of fatigue that has been persistent for at least 2 months FSS score of 4 or greater; Age 18-70. Exclusion Criteria: Use of ginseng or stimulants in the prior 6 weeks Acute treatment with glucocorticoids in the prior 6 weeks BDI >31 Significant MS exacerbation in prior 30 days Diabetes Uncontrolled hypertension Other serious medical disease, pregnancy or breastfeeding Breast disease Abnormal bleeding or clotting disorder Current use of warfarin, albendazole, nifedipine, digoxin, bumetadine, selegiline, isocarboxazid, or phenelzine Current use of lasix for poorly controlled hypertension or congestive heart failure Current drug or alcohol abuse; inability to complete the self report forms
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ruth Whitham, M.D.
Organizational Affiliation
Oregon Health and Science University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oregon Health & Science University
City
Portland
State/Province
Oregon
ZIP/Postal Code
97239
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21803872
Citation
Kim E, Cameron M, Lovera J, Schaben L, Bourdette D, Whitham R. American ginseng does not improve fatigue in multiple sclerosis: a single center randomized double-blind placebo-controlled crossover pilot study. Mult Scler. 2011 Dec;17(12):1523-6. doi: 10.1177/1352458511412062. Epub 2011 Jul 29.
Results Reference
result
PubMed Identifier
20803391
Citation
Kim E, Lovera J, Schaben L, Melara J, Bourdette D, Whitham R. Novel method for measurement of fatigue in multiple sclerosis: Real-Time Digital Fatigue Score. J Rehabil Res Dev. 2010;47(5):477-84. doi: 10.1682/jrrd.2009.09.0151.
Results Reference
derived

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American Ginseng Treatment for Multiple Sclerosis Related Fatigue

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