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OpenTrials
Completed

NCT Number: NCT03497078

Comparison of Image Quality Between New Collimator LEHRS vs Siemens LEHR on Bone Scintigraphy

Comparison of quality image with a new LEHRS GE collimator vs standard LEHR Siemens collimator on bone scintigraphy.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

CHR d'Orléans

Orléans, 45067, France

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Refered patients for scintigraphy

Exclusion criteria

  • Under 18 y. old patients
  • Pregnancy or supposed to be pregnant patients
  • Kidney failure
  • Painful patients
  • Patients under guardianship
  • Patients in whom a standard exam is not feasible

Treatment and study plan

Bone scintigraphy

Other

Comparison of image quality between new collimator LEHRS (General Electric - GE Healthcare) vs Siemens LEHR on bone scintigraphy.

Primary outcomes

  1. visual quality of bone exams

    Time frame: Day 0

Secondary outcomes

  1. Quantitative signal-noise-ratios

    Time frame: Day 0

  2. quantitative datas on phantom

    Time frame: Day 0

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Régional d'Orléans

Other

Registry information

Official study title

Comparison of Image Quality Between New Collimator LEHRS (General Electric - GE Healthcare) vs Siemens LEHR on Bone Scintigraphy

Acronym: LEHRS

Important dates

Study start
2018
Primary completion
2019
Study completion
2019
First posted
Apr 13, 2018
Registry last updated
May 6, 2019

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.