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Normal Reference Value for Echocardiography in Chinese Han Pregnancies - Trial NCT05547841

Access comprehensive clinical trial information for NCT05547841 through Pure Global AI's free database. This phase not specified trial is sponsored by First Hospital of China Medical University and is currently Recruiting. The study focuses on Pregnancy. Target enrollment is 680 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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Trial Details
ClinicalTrials.gov โ€ข NCT05547841
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Normal Reference Value for Echocardiography in Chinese Han Pregnancies
Normal Reference Value for Echocardiography in Chinese Han Pregnancies: a Prospective, Multicenter, Clinical Trial

Study Focus

Pregnancy

Echocardiography acquisition

Observational

device

Sponsor & Location

First Hospital of China Medical University

Chongqing,Chongqing,Chongqing,Haikou,Jiamusi,Nanyang,Zhengzhou,Wuhan,Wuhan,Changchun,Jilin,Jilin,Siping,Yanji,Dalian,Dalian,Fushun,Jinzhou,Jinzhou,Shenyang,Shenyang,Shenyang,Shenyang,Tieling,Yinchuan,, China

Timeline & Enrollment

N/A

Sep 01, 2022

Aug 30, 2024

680 participants

Primary Outcome

Measurement of echocardiographic parameters in Chinese Han pregnancies

Summary

The First Hospital of China Medical University initiated a multi-center study on the
 reference range of echocardiography in Chinese Han Pregnancies to determine the reference
 range of echocardiography in the pregnant population and to promote the clinical application
 of echocardiography in the pregnant population, thereby offering the value of early
 evaluation and early diagnosis for cardiac structure and function in the pregnant population.

ICD-10 Classifications

Pregnancy confirmed
Pregnancy-related condition, unspecified
Abdominal pregnancy
Pregnancy, not (yet) confirmed
Ovarian pregnancy

Data Source

ClinicalTrials.gov

NCT05547841

Device Trial