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Alzheimers Disease and Neuromarkers in Patients With Acute Hip Fractures (ADhipfract)

S

Sahlgrenska University Hospital

Status

Completed

Conditions

Inflammation
Hip Fracture
Alzheimers Disease

Study type

Observational

Funder types

Other

Identifiers

NCT02409082
HOFTDEM

Details and patient eligibility

About

The investigators explore the presence of AD factors beta-amyloid and tau in CSF and plasma to verify AD diagnosis in patients with acute hip fracture. Clinical dementia test is performed prior to operation. Blood samples and CSF samples are collected at surgery and blood samples are collected postoperatively at intervals. Mortality is assessed at 30 days, 3 months and 1 year. Morbidity is assessed at , 3 months and >1 year. Neuromarkers specifically addressing the inflammatory component are to be analyzed and correlated to outcome together with AD markers, as above.

Full description

The hypotheses explored in this investigation is that patients being pre-AD or having AD have worse prognosis following an acute hip fracture. This has been demonstrated in retrospective studies. In this study we admit all patients with a hip fracture planned tro receive a spinal anesthesia. Our golden standard of anesthesia in this patient cohort. Preoperatively Clinical Dementia Score is assessed after study inclosure. At the performance of the spinal dosage is standardized. Prior to giving this 5 ml of CSF is collected and blood is collected. Blood is then collected at intervals up until day 3 postoperatively. We plan to analyze beta-amyloid and tau in CSF and plasma to verify AD diagnosis in patients with acute hip fracture. Mortality is assessed at 30 days, 3 months and 1 year. Morbidity is assessed at, 3 months and >1 year. Neuromarkers specifically addressing the inflammatory component are to be analyzed and correlated to outcome together with AD markers, as above.

Enrollment

400 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Hip fracture with a planed spinal anesthesia

Exclusion criteria

  • Not receiving a spinal anesthesia i.e. no CSF is available

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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