- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT01547169
Study of Nasal Insulin to Fight Forgetfulness - Long-acting Insulin Detemir - 21 Days (SNIFF-LONG 21)
연구 개요
상태
상세 설명
It is well-known that insulin, a hormone that is naturally secreted by the pancreas, plays an important physiological role by regulating blood sugar levels in the body. The investigators now know that insulin plays many important roles in the brain as well. Insulin seems to be especially active in the part of the brain that corresponds to learning and memory. Studies have shown that when people have insufficient insulin in the brain (which, for example, is the case with Type-II diabetes), they are increasingly at risk to develop memory problems and Alzheimer's disease. In a past study, the investigators administered intravenous insulin to participants and found that it improves their memory. However, that particular method would not be a practical intervention for people with Alzheimer's disease due to the risk of hypoglycemia or exacerbation of insulin resistance. Instead, the investigators use an "intranasal" method of administration, in which the insulin is inserted into a device, and administered intranasally. In this method, the insulin travels directly to the brain, and bypasses the body. Our past studies have also demonstrated that this can be a reliable way to improve memory, and it does not change the body's blood glucose levels.
In our past studies, the investigators have used regular insulin, which lasts about 3-4 hours and creates a similar "spike" in insulin that one would have after eating a meal. However, in normal physiology, the pancreas also releases small and more constant "pulses" of insulin throughout the day and night, establishing a base level of insulin. Accordingly, several longer-lasting types of insulin are now available that last closer to 10-12 hours, mimicking that base level of insulin. The current study uses a long-lasting type of insulin called "insulin detemir," to determine if learning and memory will benefit from a more constant supplement of insulin. the investigators want to determine whether this treatment can benefit people who already have a memory impairment-either they already have a diagnosis of Alzheimer's disease or are diagnosed with mild cognitive impairment, a condition that precedes Alzheimer's disease, and whether a lower or higher dose of insulin detemir is more effective. The investigators will examine cognition, daily function, and different markers of Alzheimer's disease that are in the blood as outcome measures.
The investigators have these specific aims:
- The investigators will test the hypothesis that compared to placebo, three weeks of treatment with intranasal insulin detemir will improve cognition and function in adults with Alzheimer's Disease (AD) or Mild Cognitive Impairment (MCI).
- The investigators will determine which of two doses of intranasal insulin detemir produces the greatest improvement in cognition and daily function relative to placebo for adults with AD or MCI.
To examine these hypotheses, the investigators are recruiting approximately 60 participants who have been diagnosed with AD or MCI. They will be randomly selected to take a lower dose of insulin detemir, a higher dose of insulin detemir, or saline (which is an inactive substance and will serve as a placebo). Cognition and the level of daily function will be tested before they begin the study drug, and after 3 weeks of the study drug. The investigators will also measure glucose tolerance and take blood samples to measure markers of AD in the blood.
연구 유형
등록 (실제)
단계
- 2 단계
연락처 및 위치
연구 장소
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Washington
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Seattle, Washington, 미국, 98108
- VA Puget Sound Health Care System
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Age 50-89
- Diagnosed with mild cognitive impairment, or mild/moderate AD
Exclusion Criteria:
- Excessively high or low blood pressure, heart rate
- BMI greater than 34
- Pre-existing diabetes not controlled by exercise
- Previous/current use of insulin
- Significant elevations in lipids, liver enzymes
- Menstrual period within the last 12 months
- Significant neurological or medical disorder (other than AD)
- Significant use of nasal decongestants
- Current use of anti-psychotic, anti-convulsive, anxiolytic, glucocorticoids, or sedative medications
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 네 배로
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
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위약 비교기: 식염
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saline, taken twice per day for a 3 week duration
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실험적: Low Dose Insulin Detemir (10IU bid)
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10IU of insulin detemir, administered intranasally twice per day for a 3 week duration
다른 이름들:
20IU insulin detemir, administered intranasally twice per day for a 3 week duration
다른 이름들:
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실험적: High Dose Insulin Detemir (20IU bid)
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10IU of insulin detemir, administered intranasally twice per day for a 3 week duration
다른 이름들:
20IU insulin detemir, administered intranasally twice per day for a 3 week duration
다른 이름들:
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Verbal Memory Composite
기간: Change from Baseline in Verbal Memory at 3 Weeks
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The composite will consist of the weighted sum of Immediate + Delayed Story Recall and Immediate +Delayed List Recall
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Change from Baseline in Verbal Memory at 3 Weeks
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Neuropsychological Test of Executive Function 1
기간: Change from Baseline in Executive Functioning at 3 Weeks
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Computerized Dot Counting Test (test of executive functioning)
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Change from Baseline in Executive Functioning at 3 Weeks
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Glucose Tolerance
기간: Change from Baseline in Glucose Tolerance at 3 Weeks
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Subjects will undergo oral glucose tolerance test (OGTT) to assess glucose tolerance
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Change from Baseline in Glucose Tolerance at 3 Weeks
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Functional Ability
기간: Change from Baseline in Functional Ability at 3 Weeks
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Subjects will have a collateral informant (i.e., spouse or friend) rate the subjects' ability to carry out activities of daily living on the Dementia Severity Rating Scale.
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Change from Baseline in Functional Ability at 3 Weeks
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Plasma biomarkers of AD
기간: Change from Baseline in Plasma Biomarkers at 3 Weeks
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Plasma Abeta (ABeta 38, ABeta 40, and Abeta 42) and Tau (total tau and phosphorylated tau) will be measured in each subject.
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Change from Baseline in Plasma Biomarkers at 3 Weeks
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Neuropsychological Test of Executive Functioning 2
기간: Change from Baseline in Executive Functioning at 3 Weeks
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Computerized Stroop Test
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Change from Baseline in Executive Functioning at 3 Weeks
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Neuropsychological Tests of Visual Working Memory
기간: Change from Baseline in Visual Working Memory at 3 Weeks
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Benton Visual Retention Test Form F&G (a test of visual working memory)
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Change from Baseline in Visual Working Memory at 3 Weeks
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공동 작업자 및 조사자
수사관
- 수석 연구원: Suzanne Craft, PhD, VA Puget Sound Health Care System; University of Washington School of Medicine
연구 기록 날짜
연구 주요 날짜
연구 시작
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (추정)
연구 기록 업데이트
마지막 업데이트 게시됨 (추정)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .
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