Recruiting

Quetiapine

Sponsor:

University of Vermont

Code:

NCT00232570

Conditions

Alzheimer's Disease

Insomnia

Eligibility Criteria

Sex: All

Age: 55 - 70+

Healthy Volunteers: Not accepted

Interventions

quetiapine

Study Details

Brief summary:

The primary hypothesis is that quetiapine will improve sleep in persons with Alzheimer's Disease (AD), with higher doses producing greater total sleep time and sleep efficiency.

Conditions

Alzheimer's Disease

Insomnia

Study ID

NCT00232570

Start date

Nov, 2005

Status verified date

May, 2009

Completion date

Jan, 2010

Anticipated

Primary completion date

Dec, 2009

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 55 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Age 55-90 years.
2. Diagnosis of possible or probable AD as defined by NINCDS-ADRD criteria.
3. Sleep disturbance defined by mean score of 3 on first six items of the SDI.
4. Family member able to provide surrogate informed consent.
5. Live-in caregiver able to monitor medication and serve as informant on questionnaires.
6. Caregiver who is fluent in English.
7. Be able to ingest oral tablets.
8. Be able to avoid caffeinated and alcoholic beverages during the study period.
9. A neuroimaging study at the time of initial diagnosis, or any time since that is consistent with AD and effectively rules out dementia related only to stroke, hydrocephalus or other neurological condition.

Exclusion Criteria:

1. Medical disorders that may account for sleep disturbance, especially delirium, Major Depressive Disorder (DSMIV) and severe or significant acute or chronic pain.
2. Have acute or unstable medical conditions including renal failure, abnormal liver function, cardiac arrhythmia, sitting blood pressure below 110/70 or above 140/100 or postural blood drop 20 mm Hg.
3. Symptoms suggesting other sleep disorders (e.g., periodic limb movement disorder, restless legs syndrome, obstructive sleep apnea syndrome), may be present but in the opinion of the PI, do not account for the primary symptoms of insomnia.
4. Sleep disturbance symptoms that suggest a parasomnia. Parasomnias may include behavioral manifestations of epileptiform activity or REM Behavior Disorder (RBD).
5. Previous treatment failure with quetiapine of AD-associated sleep disturbances, or intolerance of quetiapine in a previous treatment trial.
6. Concomitant treatment with another antipsychotic or sedative-hypnotic medication, including trazodone.
7. Evidence of a major mental disorder other than dementia, such as major depression or schizophrenia.
8. Stable doses (for 4 weeks prior to study entry) of antidepressant, antiepileptic mood stabilizer, or acetylcholinesterase inhibitor medication will be allowed, but initiation or recent changes in the dose of such medications will be prohibited.
9. Benzodiazepines within 2 weeks of study entry will not be allowed.

Study Design

Enrollment

18 participants

Anticipated

Allocation

Non randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Interventions

quetiapine

Primary outcome measure

  • The primary objective is to determine whether quetiapine can increase total sleep time and reduce time awake in patients with AD and sleep disturbance. [ Time Frame: undefined ]

Central Contacts and Locations

Central contacts

Locations

Fletcher Allen Health Care-Clinical Neuroscience Research Unit

Recruiting

Burlington, Vermont, United States, 05401

Contacts

Principal Investigator:

Clifford Singer, M.D.

More Information

Sponsor

University of Vermont

Last update posted

May 5, 2009

Last verified

May, 2009

Keywords

  • sleep disturbance
  • dementia

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University of Vermont on 2009-05-05.