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NCT Number: NCT07483125

Valsalva SBP Drop and LVOT Obstruction

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.

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Key information

Conditions

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Zhongshan Hospital

Shanghai, Shanghai Municipality, 200032, China

Location status: Recruiting

Location contact

Yixiu Liang, PhD

CONTACT

[email protected]

+86 13566781221

About this study

Research Background

Left ventricular outflow tract obstruction (LVOTO) is a common pathophysiological change in various cardiac diseases (e.g., hypertrophic obstructive cardiomyopathy, aortic stenosis, etc.). It impedes cardiac ejection and severely affects patient prognosis.Currently, the measurement of LVOTG ≥ 30 mmHg by echocardiography is the gold standard in clinical practice for evaluating the diagnostic value of SBP waveform typing for LVOTO. However, this method is complex to operate, relies on physician experience, and does not allow continuous dynamic monitoring, which limits its application in long-term follow-up and timely adjustment of treatment regimens.Although arterial systolic blood pressure (SBP), as a key hemodynamic indicator, may be associated with the severity of LVOTO (i.e., left ventricular outflow tract gradient, LVOTG), the specific relationship, dynamic change pattern, and clinical applicability between them remain unclear.

Research Objectives

This study aims to evaluate the effectiveness of non-invasive dynamic blood flow monitoring techniques in assessing left ventricular outflow tract obstruction in patients with hypertrophic cardiomyopathy. By prospectively collecting SBP waveform and LVOTG data from patients with obstructive and non-obstructive conditions, we will systematically analyze their correlation and explore their application value in different clinical scenarios.

Study Endpoints

Primary Endpoints

① Correlation coefficient between SBP waveform characteristics and measured LVOTG values;② Sensitivity and specificity of SBP waveforms in differentiating obstructive HCM with left ventricular outflow tract obstruction.

Secondary Endpoints

① Differences in SBP waveform parameters (e.g., waveform peak, waveform duration, etc.) between obstructive and non-obstructive groups;② Consistency between SBP waveform typing and results of traditional clinical imaging methods (e.g., echocardiography);③ Incidence of procedure-related adverse events.

Study Design

This is a prospective, single-center, observational, parallel-controlled study. SBP waveform and LVOTG data will be prospectively collected from obstructive and non-obstructive patients to systematically analyze their correlation.

Gold Standard

Transthoracic echocardiography (TTE) is used as the gold standard in this study.LVOTO is defined as a resting left ventricular outflow tract peak gradient (LVOTG) ≥ 30 mmHg, or an LVOTG ≥ 50 mmHg after provocation testing (e.g., Valsalva maneuver), according to the 2020 ASE guidelines.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

1: ① Age ≥ 18 years

2: ② Diagnosed with hypertrophic cardiomyopathy (HCM) by echocardiography, with or without left ventricular outflow tract obstruction

3: ③ Conscious and mentally competent, able to understand and voluntarily sign the informed consent form

4: ④ Able to cooperate with the completion of provocation tests, non-invasive dynamic hemodynamic monitoring, and relevant follow-up examinations.

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Exclusion criteria

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

2: ② Presence of other organic heart or great vessel diseases that cause left ventricular outflow tract obstruction, such as severe aortic stenosis, congenital subaortic membrane, etc.

3: ③ Complicated with persistent atrial fibrillation or other severe arrhythmias that may affect the accuracy of hemodynamic monitoring

4: ④ Previous history of interventional or surgical therapy for left ventricular outflow tract obstruction, including septal ablation or myectomy

5: ⑤ Patients with other conditions considered inappropriate by the investigators (e.g., those with absolute or relative contraindications to provocation tests)

6: ⑥ Patients currently participating in other clinical studies.

Treatment and study plan

participants are not assigned an intervention as part of the study

Other

participants are not assigned an intervention as part of the study

Primary outcomes

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

    Time frame: 1 year

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

Study contacts

Contact information is provided by the study sponsor or research team.

Ziqing Yu, PhD

CONTACT

[email protected]

+86 18833221133

Sponsors and collaborators

Lead sponsor

Shanghai Zhongshan Hospital

Other

Registry information

Official study title

Safety and Efficacy of Non-invasive and Ambulatory Hemodynamic Monitoring for Evaluating the Left Ventricular Outflow Tract Obstruction in Hypertrophic Cardiomyopathy

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Mar 19, 2026
Registry last updated
Mar 19, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.