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OpenTrials
Completed

NCT Number: NCT04874558

Ultra-low-dose Chest CT for HHT

This study aims to develop a novel ultra-low dose chest CT technology for use in Hereditary Hemorrhagic Teleangiectasia (HHT) patients and to determine the lowest possible radiation dose that is achievable without sacrificing the diagnostic quality.

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Key information

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Ages 1 to 17 years
  • Diagnosed with positive HHT causing mutations or based on Curacao criteria

Exclusion criteria

  • Acute respiratory distress
  • Unstable cardiovascular status
  • Pneumothorax, hemoptysis
  • Pulmonary edema
  • Pulmonary emboli
  • Fractured ribs or other chest trauma
  • Recent bronchoscopy
  • Lung transplantation

Treatment and study plan

Ultra-low dose chest CT

Diagnostic Test

A novel CT technique with a new dose optimization and efficiency technology and automatic kV selection, which greatly reduces the dose of radiation exposure compared to a standard chest CT.

Primary outcomes

  1. Ultra-low dose images PAVM detection

    Time frame: Baseline

    Number of images detecting PAVM using the ultra-low dose images (50% or lower compared to the full dose)

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Official study title

Novel Ultra-low-dose Chest CT Technique to Screen for Pulmonary Arteriovenous Malformations in Pediatric Patients With Hereditary Hemorrhagic Teleangiectasia

Important dates

Study start
2021
Primary completion
2025
Study completion
2026
First posted
May 5, 2021
Registry last updated
Apr 24, 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.

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