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Not yet recruiting NCT07580872

Early Screening for Cardiac Amyloid Using a History of Bilateral Carpal Tunnel Syndrome

No phase Interventional Bilateral Carpal Tunnel Syndrome (Diagnosis) Cardiac Amyloidosis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Technetium-99m Pyrophosphate (Tc-99m PYP) Scan.
Who it may be relevant to
Registry conditions: Bilateral Carpal Tunnel Syndrome (Diagnosis), Cardiac Amyloidosis. Basic parameters: from 55 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Investigations in Early Screening for Cardiac Amyloid Through History of Bilateral Carpal Tunnel Syndrome

Overview

Cardiac amyloidosis is a condition where abnormal protein deposits build up in the heart, making it stiff and causing it to work less effectively. One common type is caused by a normal blood protein called transthyretin (TTR), which can become unstable and form these deposits. When this happens, it is called ATTR-CM, a form of heart disease caused by TTR protein buildup. This can lead to symptoms like tiredness, shortness of breath, or swelling. Bilateral carpal tunnel syndrome (CTS) is recognized as an early clinical sign of systemic amyloidosis, especially in the context of TTR amyloidosis, where amyloid deposits accumulate in the median nerve. Early identification of cardiac amyloidosis, particularly in patients with bilateral CTS, may allow for earlier intervention with disease-modifying therapies, such as tafamidis, which has been shown to improve survival and reduce hospitalizations in patients with cardiac amyloidosis. The purpose of this study is to identify patients to evaluate them for previously undiagnosed cardiac amyloidosis. The collected information will help estimate the prevalence of cardiac amyloidosis among participants with prior bilateral CTS using a PYP nuclear scan (technetium-99m pyrophosphate scan). A PYP scan is a special heart imaging test that helps doctors see if certain abnormal proteins are building up in the heart. It's mainly used to help diagnose cardiac amyloidosis.

Interventions

  • Diagnostic test Technetium-99m Pyrophosphate (Tc-99m PYP) Scan
    In this study, Technetium-99m pyrophosphate (Tc-99m PYP) cardiac scintigraphy will be performed in participants with a documented history of bilateral carpal tunnel syndrome, a recognized extracardiac manifestation associated with transthyretin (ATTR) amyloidosis. The purpose of this imaging intervention is to evaluate for the presence of cardiac transthyretin amyloid deposition in an at-risk population.

Primary outcome measures

  • Presence of Cardiac Amyloidosis [Time frame: 1 year]

Eligibility criteria

Inclusion criteria

  • Patients aged 55 and older at the time of surgery.
  • Patients who have had bilateral carpal tunnel release surgery (i.e., at least two carpal tunnel release surgeries, one for each hand).
  • Patients who underwent surgery between the years 2010-2015.

Exclusion criteria

  • Patients under the age of 55 at time of surgery.
  • Patients who had unilateral carpal tunnel release surgery or surgery on only one hand.
  • Patients known alternative neurologic diagnosis explaining CTS
  • Patients with incomplete medical records
  • Patient denies PYP scan
  • Previously diagnosed amyloidosis through previous positive PYP, medical notes or self-reported
  • Patients with prior negative amyloid work up
  • Cognitive/communication issues without available translation support

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Diagnostic

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07580872 · WREM - 126731

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗