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The Exelon Patch (Transdermal Rivastigmine) for the treatment of severe delirium in elderly subacute care inpatients

A double blinded randomised placebo controlled trial of the exelon patch (transdermal rivastigmine) for the treatment of severe delirium in elderly subacute care inpatients.

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609001020279
Acronym
EPFD1
Enrollment
60
Registered
2009-11-24
Start date
2010-02-07
Completion date
Unknown
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Acetylcholine levels are decreased in delirium, a condition of a sudden change in mental capacity occurring due to a illness, medication or similar insult. Rivastigmine is a medication for Alzhiemer's Disease, another condition where there is a change in mental capacity and low levels of acetylcholine. It increases levels of acetylcholine in the brain. THis trial aims to determine if a rivastigmine patch given to elderly patients in hospital after their illness has resolved but who still have delirium will have a less severe delirium.

Interventions

Transdermal Rivastigmine 4.6mg/hour patch applied topically changed daily for two weeks.

Sponsors

Melbourne Health
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used) (Subject, Caregiver, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Severe Delirium (Confusion assessment method positive, delirium rating scale 12 or more)

Exclusion criteria

Informed consent unable to be obtained Deficits in cardiac conducting system, resting pulse <50, intolerance or allergy to rivastigmine, carbamates or excipients. Severe dysphasia, visual or hearing impairment, or non english speaking such that unable to complete scales. Expected prognosis or discharge less than 2 weeks.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026