ClinicalTrials.Veeva

Menu

Prevalence of Wildtype Amyloid After TAVR

N

North Florida Foundation for Research and Education

Status

Withdrawn

Conditions

Amyloidosis

Study type

Observational

Funder types

Other

Identifiers

NCT03825406
#: 201802928

Details and patient eligibility

About

Those with abnormal vital signs after TAVR need to be willing to obtain a bone scan to evaluate for wildtype amyloidosis. Positive bone scan findings will require evaluation for primary amyloidosis with blood and urine monoclonal immunoglobulin testing. Primary amyloidosis is a different type of disease which requires different treatment.

Full description

This research is interested in determining how common wildtype amyloidosis is after transcatheter aortic valve replacement (TAVR). Amyloidosis is a condition characterized by abnormal protein which can accumulate and impair various organs, including the heart. Research suggests that amyloidosis might be common among TAVR patients, but it is a condition that is not routinely evaluated for. We suspect that wildtype amyloidosis may be especially common among patients with abnormal vital signs after their TAVR procedure.

Sex

All

Ages

50 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria

  • Patients that underwent a TAVR procedure at the Malcolm Randall VA Medical Center.
  • Implant of current generation TAVR (i.e. Sapien S3, Evolut R, or Evolut Pro).
  • Willingness to obtain bone scintigraphy if evidence of impaired hemodynamics after valve deployment.
  • Willingness to have blood drawn
  • Willingness to complete SF12 quality of life KCCQ

Exclusion Criteria:

--Patient that do not qualify for a TAVR procedure as normal clinical care

Trial contacts and locations

0

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2024 Veeva Systems