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Not yet recruiting NCT07267533

Precise 3D Surview

Observational Computed Tomography

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Computed Tomography. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Precise 3D Surview Clinical Study

Overview

The purpose of the study is to assess the performance of Precise 3D Surview on CT 5300 and Incisive CT Scanners as compared with manual annotation by experienced CT technologists. * To evaluate the acceptance rate of the Auto 3D Planning Box compared with manual annotation by experienced CT technologists. * To evaluate the acceptance rate of the Auto Suggestion for Locator compared with manual annotation by experienced CT technologists. * To evaluate the acceptance rate of the Auto Planning for Truncated Anatomies (lung and liver) compared with manual annotation by experienced CT technologists. * To evaluate the acceptance rate of Auto Planning and Symmetry Correction for Tilted Head compared with manual annotation by experienced CT technologists.

Primary outcome measures

  • Acceptance rate of the 3D Surview [Time frame: Reading session at 4 months]

Eligibility criteria

Inclusion criteria

  • Subjects scanned by CT 5300 (K232491) and Incisive CT (K212441) according to the department standard of care clinical protocols.
  • Subjects age is over eighteen (18) years1.
  • Patients scanned in supine orientation.
  • Non-contrast CT scan
  • CT scan with standard resolution

Exclusion criteria

  • Subjects age is under or equal 18 years old
  • Patients are not scanned in supine orientation.
  • Contrast-enhanced CT scans.
  • CT scans with high resolution
  • Scans that are not completed due to technical difficulties

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT07267533 · Precise 3D Surview

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗