ClinicalTrials.Veeva

Menu

Enhanced CJD Surveillance in the Older Population

U

University of Edinburgh

Status

Completed

Conditions

Prion Disease
Dementia

Treatments

Other: Blood or buccal sample
Other: Participant follow-up
Other: Post mortem examination
Other: Clinical assessment and review
Other: Medical history questionnaire

Study type

Observational

Funder types

Other

Identifiers

NCT02629640
15/SS/0196

Details and patient eligibility

About

The purpose of this study to investigate if cases of Creutzfeldt-Jakob Disease (CJD) and other forms of prion disease are being missed in older adults living within Lothian.

Full description

The study involves patients aged 65 years or over who have been seen by a neurologist or psycho-geriatrician and identified as having features that are atypical for the known types of dementia. All patients will be invited to an initial meeting with the research team to discuss the study and, if they agree to participate, for clinical assessment and epidemiological review. Participants will be asked to donate blood or a buccal sample for codon-129 polymorphism genotyping and may be offered a MRI brain scan if no such imaging has been previously undertaken. Participants will also be asked to consider if, in the event of their death, they would donate samples of brain tissue to the Edinburgh Brain Bank for use in this and future research. Telephone follow up will be offered within 1 month of joining the study and at 3 monthly intervals thereafter, with further clinical review offered if deemed appropriate.

Enrollment

30 patients

Sex

All

Ages

65+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients aged 65 years or above
  • Patients accessing NHS Lothian neurology and psychogeriatric services
  • Patients who have features atypical for the recognised forms of dementia
  • Appropriate informed consent

Exclusion criteria

  • Patients aged below 65 at time of recruitment
  • Patients diagnosed with a clear alternative demonstrable pathology

Trial design

30 participants in 1 patient group

Research Participants
Description:
Medical history questionnaire; clinical assessment and review; participant follow-up; blood or buccal sample; post mortem examination.
Treatment:
Other: Clinical assessment and review
Other: Medical history questionnaire
Other: Post mortem examination
Other: Participant follow-up
Other: Blood or buccal sample

Trial contacts and locations

1

Loading...

Central trial contact

Lovney Kanguru

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems