跳至主要内容
临床试验/NCT03503331
NCT03503331招募中2 期

UAB Alzheimer's Disease Center Core Cohort - Imaging Substudy

University of Alabama at Birmingham2 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2018年4月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
招募中
入组人数
160
试验地点
2
主要终点
Measurement of pathological beta-amyloid in the brain

研究概览

简要总结

The primary objective of this study is to measure the concentration and the regional brain distribution of pathologic amyloid deposition using the PET tracer [C-11]PiB in participants in the UAB Alzheimer's Disease Center cohort. Assessment of interactions between race and vascular risk factors, brain amyloid levels measured with [C-11]PiB-PET, and cognitive status will be the primary outcome of this imaging study.

详细描述

The primary objective of this study is to measure the concentration and the regional brain distribution of pathologic amyloid deposition using the PET tracer [C-11]PiB in participants in the UAB-ADC cohort. The amount and distribution of [C-11]PiB in the brain will be correlated to demographic, clinical, genetic, and biospecimen data acquired through the separate ongoing UAB-ADC study. Assessment of interactions between race and vascular risk factors, brain amyloid levels measured with [C-11]PiB-PET, and cognitive status will be the primary outcome of this imaging study. As a secondary aim, the investigators will assess the ability of the early flow frames from [C-11]PiB-PET and brain volumetric measurements with MRI to serve as a marker of neuronal injury and to predict cognitive status in conjunction with the amyloid-PET results.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

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

入选标准

  • Enrollment in the UAB-ADC study under a separate IRB-approved research protocol (IRB-300000169).
  • 2. Negative urine or serum B-hCG test within 2 days of [C-11]PiB administration in women of child bearing potential. Women who are post-menopausal with at least 1 year since last menses or documented surgical sterilization will not require pregnancy testing.

排除标准

  • Meets any exclusion criteria for the UAB-ADC study (IRB-300000169).
  • Inability or contraindication for undergoing MRI and/or PET imaging
  • Inability to participate in the imaging studies due to severity of dementia

研究组 & 干预措施

[C-11]PiB-PET/MRI

Experimental

All participants in this study will undergo an amyloid-PET imaging using the tracer [C-11]PiB with a simultaneous PET/MRI system. The [C-11]PiB dosage is 300-670 MBq (8 - 18 mCi) given intravenously, and the PET/MRI imaging time is approximately 60 min.

干预措施: [C-11]PiB-PET/MRI (Drug)

结局指标

主要结局

Measurement of pathological beta-amyloid in the brain

时间窗: 5 years

The amount of pathological beta-amyloid in the brains of study participants will be measured with \[C-11\]PiB-PET/MRI using standardized uptake value ratios (SUVRs) derived from the PET images.

次要结局

未报告次要终点

研究者

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

Deepak Prabataram Kalbi

Assistant Professor

University of Alabama at Birmingham

研究点 (2)

Loading locations...

相似试验

进行中(未招募)
不适用
Vaginal ring dysmenorrhea feasibility trial.
EUCTR2012-002449-40-DKMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.450
进行中(未招募)
不适用
Vaginal ring dysmenorrhea feasibility trial.This study will investigate the use of 4 doses of combined contraceptives (a progestin with an estrogen) in a vaginal ring dosage form for the treatment of dysmenorrhea (menstrual cramping pain). A placebo control arm will also be utilized.MedDRA version: 14.1Level: LLTClassification code 10013934Term: DysmenorrheaSystem Organ Class: 100000004872
EUCTR2012-002449-40-PLMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.450
进行中(未招募)
不适用
Vaginal ring dysmenorrhea feasibility trial.
EUCTR2012-002449-40-SEMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.450
进行中(未招募)
1 期
Vaginal ring dysmenorrhea feasibility trial.This study will investigate the use of 4 doses of combined contraceptives (a progestin with an estrogen) in a vaginal ring dosage form for the treatment of dysmenorrhea (menstrual cramping pain). A placebo control arm will also be utilized.MedDRA version: 15.0 Level: LLT Classification code 10013934 Term: Dysmenorrhea System Organ Class: 10038604 - Reproductive system and breast disorders
EUCTR2012-002449-40-NOMerck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.439
已完成
2 期
A multicenter, randomized, partially blinded, placebo-controlled clinical trial to evaluate the effect on primary dysmenorrheal of vaginal rings with an average daily release of 700 µg nomegestrol acetate (NOMAC) and 300 µg estradiol (E2), or 900 µg nomegestrol acetate (NOMAC) and 300 µg estradiol (E2), or 100 µg etonogestrel (ENG) and 300 µg E2, or 125 µg etonogestrel (ENG) and 300 µg E2primaire dysmenorroe + reproductive system and breast disorders (menstrual cycle and uterine bleeding disorders)pain and/or cramps during menstruation
NL-OMON36928Merck Sharp & Dohme (MSD)35