CompletedPhase 2ACTRN12609000975291

A randomised double blind, placebo-controlled study of Nefiracetam in patients with post- stroke apathy

In post stroke patients, treatment with nefiracetam decreases the severity of apathy


Sponsor

Fremantle Hospital and Health Service

Enrollment

122 participants

Start Date

Jul 27, 2010

Study Type

Interventional

Conditions

Summary

The successful psycho-physical rehabilitation of stroke victims remains challenging. Recent advances have resulted in progress in acute treatment of stroke, however post-acute rehabilitation remains basically unchanged. One reason for this is the high frequency of emotional and behavioural disorders post-stroke, such as apathy. Apathy is associated with greater deficits in activities of daily living, more severe cognitive deficits, longer hospital stay, and worse rehabilitation and functional outcomes. There are no known effective pharmacological or psychological treatments for apathy after stroke. We aim to determine if treatment with nefiracetam decreases the severity of post-stroke apathy. We will also test whether nefiracetam results in greater improvement on functional and social impairments, quality of life and cognition as compared to placebo.


Eligibility

Sex: Both males and femalesMin Age: 40 YearssMax Age: 90 Yearss

Plain Language Summary

Simplified for easier understanding

This study tests a medication called Nefiracetam for treating apathy (loss of motivation and interest) that can develop after a stroke. It is for adults aged 40 to 90 who have experienced a stroke and developed apathy afterward, and who do not have major depression.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

450mg Nefiracetam (one capsule orally) twice daily for 12 weeks

450mg Nefiracetam (one capsule orally) twice daily for 12 weeks


Locations(1)

WA, Australia

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ACTRN12609000975291