Effect of Indomethacin on the Progression of Alzheimer's Disease

• Status: Completed
• Trial end date: 2005-08-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is determine whether indomethacin is able to retard disease progression in patients with mild to moderate Alzheimer's disease.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Radboud University
• Collaborators: American Health Assistance Foundation; Netherlands Alzheimer Foundation; Netherlands Brain Foundation
• Treatments: Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non-Steroidal; Indomethacin

Criteria

Inclusion Criteria:

• The patient will satisfy the DSM-IV criteria for dementia of the Alzheimer's type.

• The patient will satisfy the NINCDS/ADRDA criteria for the clinical diagnosis of probable Alzheimer's disease (Appendix I).

• The severity of dementia for each patient will be quantified by a Mini-Mental State Examination (MMSE) score between 10 and 26 (both inclusive).

• The patient is living at home or in a home for the elderly.

• The patient has a responsible caregiver who is able to provide information about the patient's functional status.

• Written informed consent is obtained from the patient or the legally accepted representative.

Exclusion Criteria:

• The patient satisfies the NINDS-AIREN criteria for probable vascular dementia.

• A known exaggerated pharmacological sensitivity or allergy to NSAID's.

• History of peptic ulceration, gastric surgery or gastrointestinal bleeding.

• Current diagnosis of active peptic ulceration.

• Current diagnosis of severe and unstable cardiovascular disease.

• Current diagnosis of renal failure.

• Advanced, severe and unstable disease of any type, other than Alzheimer's disease, that may interfere with primary and secondary variable evaluations, including a medical condition which should be expected to progress, recur, or change to such an extent that it may bias the assessment of the clinical or mental status of the patient to a significant degree or put the patient at special risk.

• Intake of any of the following concomitant medications: salicylates, coumarin derivatives, ACE-inhibitors, loop diuretics.

• Intake of any of the following concomitant medications more than two months immediately prior or during the study: NSAID's, systemic corticosteroids.

• Intake of any of the following concomitant medications with a possible effect on cognition: estrogen, deprenyl, vitamin E, neuroleptics, anticholinergics. Patients using stable doses of cholinesterase inhibitors were eligible, with the provision that the dose should not be changed during the study. Cholinesterase inhibitors could not be initiated during the study.

• Excessive use of alcohol (more than 5 units per day)

• The patient is, either alone or with the aid of a caregiver, not able to reliably take the medication.