Study of Ginseng in Treatment of Fatigue in Multiple Sclerosis

CompletedPhase 2Relapsing MSNCT01712373

What it found

Met its main goal

The main measure showed a statistically significant benefit.

“Statistical analysis showed better effects for ginseng than the placebo as regards MFIS (p = 0.046) and MSQOL (p ≤ 0.0001) after 3 months.”
Read by software from the paper's abstract

3 months

p = 0.046

Total participants: 60

Read by software from the paper's abstract

This trial finished 15 years ago. We found no results in the registry or in any paper that cites it.

What was tested

Treatment tested

  • Ginseng, asian

Placebo

  • Placebo

What it measured

Main measures

  • Fatigue

    at 3 months after treatment

    Thinking and memoryFatigue

Other measures (1)

  • Quality Of Life

    at 3 months after treatment

    Quality of life (reported by participants)

Who could take part

Relapsing MS · 18 to 50

Show the full criteria

Inclusion criteria

* definite diagnosis of relapsing-remitting MS (RRMS) by the MacDonald criteria with a baseline of Expanded Disability Status Score (EDSS)of less than 5.0

Exclusion criteria

* prior use of ginseng or any other tonic agents, glucocorticoids, warfarin, digoxin, aspirin, furosemide, caffeine, ephedra and anti-platelet agents within one month prior to enrollment; * Pregnancy or lactation; * history of renal failure; and, * lack of appropriate adherence to the study protocol.

As registered. Criteria can change, so ask the trial team or your neurologist.

About this trial

In the sponsor's words

The purpose of this study was to evaluate the efficacy and safety of Ginseng in treatment of fatigue and Quality of Life of MS patients.

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History

    1. Started

      Dec 2010

    2. Main results due

      Apr 2011

    3. Finished

      Apr 2011

    Assembled by software from public sources.