Valsalva SBP Drop and LVOT Obstruction

ConditionsHCMoHCMnHCM
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorShanghai Zhongshan Hospital

About this trial

This study aimed to evaluate the efficacy of non-invasive dynamic blood pressure monitoring in assessing left ventricular outflow tract obstruction in patients with hypertrophic cardiomyopathy. We prospectively collected SBP waveforms and LVOT gradient data from patients with obstructive and non-obstructive disease, systematically analyzed their correlation, and explored its clinical value in different clinical scenarios.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

1: ① Age ≤ 18 years, or pregnant/lactating patients

Trial population

HCM patients: In this study, transthoracic echocardiography (TTE) was used as the gold standard. Left ventricular outflow tract obstruction (LVOTO) was defined as a resting left ventricular outflow tract gradient (LVOTG) ≥ 30 mmHg, or an LVOTG ≥ 50 mmHg after provocation tests (e.g., Valsalva maneuver), according

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • participants are not assigned an intervention as part of the study

    Other intervention

    participants are not assigned an intervention as part of the study

Treatment groups

800 Participants
are divided into 1 treatment group
Group A: HCM1 intervention

Trial outcomes

Primary outcomes

1

Sensitivity and specificity of SBP waveform in differentiating obstructive HCM caused by left ventricular outflow tract obstruction

Sensitivity and specificity of SBP waveform in differentiating obstructive HCM caused by left ventricular outflow tract obstruction

Time frame
1 year

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.