CompletedPhase 3MS (type not specified)NCT00139789

What it found

No result found

We found no results in the registry or in papers.

This trial finished 21 years ago. We found no results in the registry or in any paper that cites it.

What was tested

Treatment tested

Who could take part

MS (type not specified) · 18 to 65

Inclusion Criteria: * stable dose of baclofen Exclusion Criteria: * not stable dosing

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

About this trial

In the sponsor's words

This was a multicenter, open-label, randomized, crossover trial in subjects with MS who were already taking a stable dose of baclofen (up to 80 mg/day) for spasticity. The trial was designed to assess subject preference for Kemstro or conventional baclofen. At Visit 1, subjects were screened, and if qualified, were randomly assigned to one of two following treatment sequences: Kemstro/conventional baclofen or conventional baclofen/Kemstro.

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History

    1. Started

      Jan 2005

    2. Main results due

      Apr 2005

    3. Finished

      Apr 2005

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