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Donepezil Memory Preservation Post ECT

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Porter Adventist Hospital

关键词

抽象

This randomized, placebo-controlled trial will evaluate the use of donepezil compared to placebo to reduce the risk of memory impairment after electroconvulsive therapy (ECT).

描述

Electroconvulsive therapy (ECT) is a method used to treat a variety of psychiatric conditions. An electrical current is distributed throughout the brain (Lisanby 2007) inducing seizure activity in a controlled setting using neuromuscular blocking agents (Mirzakhani 2012) while the patient is under anesthesia (Deiner 2009). ECT is approved by the Food and Drug Administration (FDA) for the following conditions: unipolar and bipolar depression, manic and mixed states in bipolar disorder, schizophrenia, schizoaffective disorder, schizophreniform disorder and catatonia (FDA executive summary). ECT is often used after trials of psychotropic medications have failed (Kellner 2012).

Electroconvulsive therapy (ECT) is commonly associated with cognitive side effects that range from anterograde and retrograde amnesia to issues with executive function, attention and declines in information processing. Problems with autobiographical memory and recall for new information appear to be affected the most. In addition, data suggests that the loss of memory of autobiographical events may persist as long as six months. These issues may cause patient adherence problems and potential relapses into previous psychiatric conditions.

Donepezil is an acetylcholinesterase inhibitor indicated for Alzheimer's Dementia and has been shown to slow the progressive decline in cognition and memory in Alzheimer's Dementia. It is hypothesized that donepezil will help to preserve memory and minimize the decline in memory that is associated with the administration of ECT.

This study aims to determine if donepezil can minimize deficiencies in autobiographical memory 4-5 weeks after ECT treatment has been started.

日期

最后验证: 06/30/2018
首次提交: 12/30/2014
提交的预估入学人数: 01/01/2015
首次发布: 01/05/2015
上次提交的更新: 07/02/2018
最近更新发布: 07/05/2018
实际学习开始日期: 09/23/2015
预计主要完成日期: 01/24/2017
预计完成日期: 03/23/2017

状况或疾病

Memory Impairment

干预/治疗

Drug: donepezil

Drug: Placebo

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手臂组

干预/治疗
Active Comparator: donepezil
Subjects will receive donepezil 5 mg before before they start ECT and continue the agent through the ECT procedures up to 4 weeks.
Drug: donepezil
Donepezil 5 mg once daily 2 days before ECT and continuing through the last ECT procedure.
Placebo Comparator: Placebo
Subjects will receive the placebo before they start ECT and continue the agent through the ECT procedures up to 4 weeks.
Drug: Placebo
Placebo capsule once daily 2 days before ECT and continuing through the last ECT procedure.

资格标准

有资格学习的年龄 18 Years 至 18 Years
有资格学习的性别All
接受健康志愿者
标准

Inclusion Criteria:

- Diagnosis of major depressive disorder, anxiety disorders, bipolar depression who are receiving right unilateral ECT will be included.

Exclusion Criteria:

- Patients with previous use of alcohol or illicit drugs within seven days of randomization will be excluded. Preexisting unstable cardiovascular disease including uncontrolled hypertension will be excluded. Patients with a documented allergy to donepezil will also be excluded. Patients with axis I disorders (eg. schizophrenia, schizoaffective disorder) other than major depressive disorder, anxiety disorders and/or bipolar depression will be excluded. Patients on anticoagulant therapy or chronic NSAID therapy will be excluded. Patients who are pregnant or wish to become pregnant within one year from trial enrollment will also be excluded. Patients who have received ECT within 6 months of enrollment will be excluded. Baseline Mini Mental State Examination (MMSE) < 24 will be excluded.

结果

主要结果指标

1. Columbia University Autobiographical Memory Interview-Short Form (AMI-SF) [4-5 weeks after first ECT treatment]

次要成果指标

1. Short Term Memory Four-Word MemoryTask [4-5 weeks after first ECT treatment]

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