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OpenTrials
Completed

NCT Number: NCT03589664

CT Data Collection Study

The primary objective of this study is to gather chest CT images as part of routine clinical procedure from subjects with and without prior sternotomy to characterize the substernal space. Specifically, the study will provide references for physicians to better understand substernal anatomy.

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Key information

Age range

18 year–80 year

Sex eligibility

All sexes

Study type

Observational

Primary location

TongRen Hospital, Shanghai Jiao Tong University School of Medicine

Shanghai, China

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Subject must be≥18 years old
  • Subject must be indicated for high quality chest CT imaging as part of routine clinical procedure
  • Subject must be willing to provide Informed Consent

Exclusion criteria

  • Subject has medical conditions that would limit study participation
  • Subject is pregnant or have a pregnancy plan during the study
  • Subject is enrolled in a concurrent study that may confound the results of this study

Treatment and study plan

Primary outcomes

  1. CT imaging data

    Time frame: At enrollment

    High quality CT images

Sponsors and collaborators

Lead sponsor

Medtronic Cardiac Rhythm and Heart Failure

Industry

Registry information

Official study title

Computed Tomography Data Collection for Anatomical Analysis of Substernal Space in Patients With Cardiovascular Diseases

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Jul 18, 2018
Registry last updated
Oct 14, 2020

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.

Published trials that share one or more normalized conditions with this study.