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临床试验/NCT00065169
NCT00065169已完成不适用

Anti-Inflammation in AD: PET Imaging Supplement

University of California, Los Angeles2 个研究点 分布在 1 个国家目标入组 138 人开始时间: 2000年11月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
138
试验地点
2

研究概览

简要总结

The purpose of this study is to determine whether the anti-inflammatory drug celecoxib can delay the onset of Alzheimer Disease (AD) in people with Age Associated Memory Impairment (AAMI). This study will also evaluate genetic risk and brain structure as potential predictors of mental decline.

详细描述

AD is one of the most common mental disorders of late life. Preliminary studies indicate that anti-inflammatory drugs may attenuate or prevent AD symptoms, but efficacy trials are needed.

Participants in this study will be randomly assigned to receive either celecoxib or placebo for 18 months. Participants will undergo positron emission tomography (PET) and magnetic resonance imaging (MRI) scans of the brain. Routine laboratory blood tests, cognitive tests, and an electrocardiogram (ECG) will be performed. Participants will also be screened for Parkinson disease. Follow-up testing will be conducted at specific intervals following the study.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Double

入排标准

年龄范围
40 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • NIMH diagnostic criteria for Age Associated Memory Impairment (AAMI)
  • Mini-Mental State Examination (MMSE) score between 26 and 30 (unless < 8 years of educational achievement)
  • No significant cerebrovascular disease
  • Estrogen replacement therapy and thyroid replacement therapy (if the participant is euthyroid) are permitted if the therapies are stable for > 1 month
  • Memory and verbal fluency cut-off scores that increase the probability of incipient dementia (Buschke-Fuld: 34; verbal fluency: 46 for letters, 7 for categories; Benton Visual Retention: 5)
  • Adequate visual and auditory acuity to allow neuropsychological testing
  • Normal screening laboratory tests and electrocardiogram (ECG)

排除标准

  • Possible or probable Alzheimer Disease (AD) or other dementia
  • Neurologic or other physical illness that could produce cognitive deterioration
  • History of transient ischemic attacks (TIAs), carotid bruits, or lacunes on an MRI scan
  • History of myocardial infarction within the previous year or unstable cardiac disease
  • Uncontrolled hypertension (systolic BP > 170 or diastolic BP > 100)
  • History of significant liver disease, pulmonary disease, diabetes, or cancer
  • DSM-IV criteria for major psychiatric disorders within the previous 2 years
  • Past or present history of alcoholism or drug dependence
  • Untreated depression as determined by a Hamilton Depression Rating Scale (HAM-D) score of 12 or more
  • Drugs that may significantly affect psychometric test results
  • Centrally active beta-blockers, narcotics, clonidine, anti-Parkinsonian medications, antipsychotics, benzodiazepines, systemic corticosteroids, medications with significant cholinergic or anticholinergic effects, anti-convulsants, warfarin, vitamins other than the standard multivitamin supplement, ginkgo biloba, and any nutraceuticals. Occasional chloral hydrate use will be allowed, but discouraged, for insomnia.
  • Investigational drugs within the previous month or longer, depending on drug half-life
  • Contraindication for MRI scan (e.g., metal in body, claustrophobia)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Gary Small, MD

UCLA Professor of Psychiatry and Biobehavioral Sciences

University of California, Los Angeles

研究点 (2)

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