Delirium Clinical Trial
Official title:
Rivastigmine for the Prevention of Postoperative Delirium After Cardiac Surgery
Verified date | July 2007 |
Source | University Hospital, Basel, Switzerland |
Contact | n/a |
Is FDA regulated | No |
Health authority | Switzerland: Swissmedic |
Study type | Interventional |
The purpose of this study is to determine whether Rivastigmine is effective for the prevention of postoperative delirium in patients undergoing cardiac surgery.
Status | Completed |
Enrollment | 120 |
Est. completion date | July 2007 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 65 Years and older |
Eligibility |
Inclusion Criteria: - Patients undergoing cardiac surgery with use of extracorporeal circulation - Aged 65 or more Exclusion Criteria: - "redo" procedures - anticipated use of succinylcholine during operation - contraindications to rivastigmine - preoperative mini mental score < 15 |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
Switzerland | University Hospital Basel | Basel |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Basel, Switzerland | Novartis |
Switzerland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Development of postoperative delirium within 7 days after cardiac surgery | |||
Secondary | Severity of delirium occurring within 7 days after cardiac surgery | |||
Secondary | Length of stay (intensive care and hospital) | |||
Secondary | Amount of drugs used for rescue therapy of delirium |
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