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Rivastigmine as a treatment in delirium; a pilot study

Delirium after stroke and treatment with rivastigmine; a pilot study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON28018
Enrollment
20
Registered
2008-08-05
Start date
2004-02-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

delirium stroke (dutch

Interventions

Rivastigmine 1.5 b.i.d, with an increase every other day with 3 mg to a maximum of 6 mg b.i.d

Sponsors

Novartis
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Recent stroke 2. Persistent delirium 3. Severe delirium

Exclusion criteria

Exclusion criteria: 1. Prior adverse effects of rivastigmine 2. Severe renal failure 3. Age < 18 years 4. Women of child bearing potential 5. Use of any other investigational agent in the last 30 days

Design outcomes

Primary

MeasureTime frame
Presence of delirium measured with confusion assessment method and delirium rating scal

Secondary

MeasureTime frame
- Duration of delirium - Other medication needed

Contacts

Public ContactG. Roks

St Elisabeth Hospital Department of Neurology PO box 90151

g.roks@elisabeth.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)