Clinical trial

Effect of Acetylcholinesterase Inhibitors on Bone Metabolism and Fracture Risk Factors Among Older Adults With Mild to Moderate Alzheimer's Disease

Name
Pro00111080
Description
People with Alzheimer's disease are at an increased risk of bone fracture. Some studies have shown that those taking donepezil have a lower rate of bone fractures, but the reasons for this are unknown. The purpose of this study is to measure the effect of donepezil treatment on bone metabolism factors including bone mineral density, bone turnover markers, and bone quality. Participants in this study will have a bone density test and have blood samples collected at the baseline study visit. Participants will then be randomly assigned to donepezil or matching placebo to be taken daily by mouth for 12 months. Blood samples will be collected at 6 and 12 months. A repeat bone density test will be performed at 12 months. Participants will also complete questionnaires at each study visit.
Trial arms
Trial start
2024-07-01
Estimated PCD
2025-06-01
Trial end
2025-06-01
Status
Not yet recruiting
Phase
Early phase I
Treatment
Donepezil
10 mg tablet
Arms:
Donepezil
Placebo
Donepezil placebo tablet
Arms:
Placebo
Size
45
Primary endpoint
Change in bone mineral density, as measured by dual x-ray absorptiometry (DXA)
baseline, 12 months
Eligibility criteria
Inclusion Criteria: 1. Diagnosis of ADRD, including clinical assessment and either radiographic or laboratory biomarker assessment 2. Meets NIA-AA clinical dementia criteria 3. Willing to initiate treatment with AchEI for ADRD 4. MoCA score \< 24 5. For females, either age \> 55 years, or Age \< 55 years and at least 12 months since last menstrual period 6. For males, age \> 50 years 7. Geriatric Depression Scale score \< 6 Exclusion Criteria: 1. Currently on acetylcholinesterase inhibitor 2. Currently on osteoporosis medication (e.g., bisphosphonate, SERM, denosumab, teripar-atide, abaloparatide, romozosumab) 3. Use of bisphosphonate within last 2 years 4. Use within last 6 months of estrogens or testosterone, androgen deprivation therapy or aromatase inhibitors, antiepileptic, heparin therapy, thiazolidinediones 5. History of disorders associated with osteoporosis: collagen vascular diseases, malab-sorption, inflammatory bowel disease, severe liver disease/cirrhosis, hyperthyroidism (endogenous or exogenous) 6. History of hip fracture, hip replacement, or non-ambulatory 7. Long-term use (\>6 months) of corticosteroids 8. History of Parkinson's, HIV, Huntington's disease 9. History of solid organ transplantation 10. Severe kidney impairment (eGFR \< 30 ml/sec), 11. Active malignancy, except non-melanomatous skin cancer 12. 1-year mortality \> 25%, measured by ePrognosis calculator 13. Initiation of investigational or FDA-approved anti-amyloid drug
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 45, 'type': 'ESTIMATED'}}
Updated at
2024-05-20

1 organization

2 products

1 indication

Organization
Duke University
Product
Donepezil
Indication
Osteoporosis
Product
Placebo