About this trial
Study participants will be prospectively recruited from consecutive outpatient and inpatient populations presenting to the Cardiology and Cardiac Surgery Departments of the following participating institutions: The First Affiliated Hospital of Xi'an Jiaotong University, The Second Affiliated Hospital of Xi'an Jiaotong University, and \[add additional participating institutions as applicable\].
Eligibility criteria
Qualifiers
- Aged ≥ 18 years.
For the case group: Presence of valvular lesions confirmed by transthoracic echocardiography.
For the control group: Normal cardiac valves and no evidence of other cardiovascular diseases confirmed by transthoracic echocardiography.
Ability to undergo and complete speckle tracking echocardiography.
Disqualifiers
Patients who are unwilling to participate in this study.
Patients with a known allergy to the electrode patches or medical adhesive tapes used in this study.
Patients who are unable to cooperate with the completion of required examinations.
Patients with incomplete clinical or imaging data that cannot be supplemented.
Trial design
Treatments tested in this trial
- Transthoracic Echocardiography
Treatment groups
Locations
Sponsors and collaborators
First Affiliated Hospital Xi'an Jiaotong University
Lead sponsor
Second Affiliated Hospital of Xi'an Jiaotong University
Collaborator