Skip to main content
Delfa

← Trials/Trial dossier/NCT00000179

CompletedPhase 3

Agitation in Alzheimer's Disease

Assets

Haloperidol / Trazodone

Listed sites

16

Recruiting sites

-

Enrollment

-

Study population

Alzheimer’s disease

Key I/E criteria

Alzheimer's diseaseStudy partner/caregiver required

Primary endpoint

-

Footprint

Where this trial recruits

Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

Nih3U01AG010483-08S2
Org study IDIA0003
NCT IDNCT00000179

Timeline

Milestones

Study first posted1999-11-01estimated
Last update posted2005-06-24estimated

Assets

Drug assets

Study populations

Who this study enrolls

Alzheimer’s disease

Eligibility

Who can enroll

Minimum age50 Years
SexAll
Healthy volunteersNot accepted

Eligibility criteria

Memory problem consistent with a probable diagnosis of Alzheimer's disease (AD)
Agitation symptoms for at least the past 2 weeks
Patient has caregiver who can participate
Patient lives in the same household as the caregiver

Endpoints (0)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

No endpoints recorded for this trial.

Publications (1)

Bibliography

Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 21, 2026
Endpoint classificationDelfa ADRD endpoint taxonomy
Results tableno registry results posted yet

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 21, 2026 snapshot.