Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
NCT05566002

Artificial Intelligence-assisted Evaluation of Pulmonary HYpertension

Led by Chinese Pulmonary Vascular Disease Research Group · Updated on 2025-04-08

2000

Participants Needed

1

Research Sites

187 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Pulmonary hypertension represents a challenging and heterogeneous condition that is associated with high mortality and morbidity if left untreated. Artificial intelligence is used to study and develop theories and methods that simulate and extend human intelligence, which is being applied in fields related to cardiovascular diseases. The study intends to combine multimodal clinical data of patients who undergo right heart catheterization at Fuwai Hospital with artificial intelligence techniques to create programs that can screen and diagnose pulmonary hypertension.

CONDITIONS

Official Title

Artificial Intelligence-assisted Evaluation of Pulmonary HYpertension

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 6518 years old
  • Patients previously received chest X-ray, electrocardiography, echocardiography, other routine examinations, and right heart catheterization at the Fuwai Hospital, CAMS & PUMC, Beijing, China
Not Eligible

You will not qualify if you...

  • Patients without right heart catheterization
  • The quality of routine examinations and right heart catheterization cannot meet the requirement for further analysis
  • Severe loss of results of routine examinations (chest X-ray, electrocardiography, echocardiography, etc.)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Fuwai Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

Beijing, Beijing Municipality, China, 100037

Actively Recruiting

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Research Team

Z

Zhihong Liu, MD, PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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