Spectral Precise Image Study for Brain Tumors
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
- The protocol lists: This is an observational data collection study.
- Who it may be relevant to
- Registry conditions: Brain Tumors. 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
- China
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Clinical Study for Exploring Image Quality the Spectral Precise Image in Patients With Diagnosed Intracranial Tumors
Overview
The goal of this observational study is to explore the image quality of spectral CT deep learning reconstruction technology (Spectral Precise Image) of patients with confirmed brain tumors. The main question it aims to answer is: The Image Quality (IQ) and diagnostic confidence of Spectral Precise Image reconstructions
Interventions
- Device This is an observational data collection study
This is an observational data collection study
Primary outcome measures
- Subjective Image quality using Likert score (1-5) [Time frame: From date of image reconstruction until the date of image reading completion, anticipated 3Months.]
- Objective Image Quality [Time frame: From date of image reconstruction until the date of image reading completion, anticipated 3Months.]
Eligibility criteria
Inclusion criteria
- Patients with clinical and radiology (MRI/CT) diagnosed brain tumors.
- Patients who underwent contrast enhanced scans using the Spectral CT 7500.
- Study participants with age ≥ 18 years old.
- Study participants that have signed Informed Consent Form (ICF)
Exclusion criteria
- The clinical data or radiological information is considered incomplete after evaluation by the investigator.
- Study participant that was enrolled in this study in the past
- Data from study participants deemed unsuitable for enrollment based on the investigator's evaluation
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Case-only
Study locations
China · 1 center
- Union Hospital, Tongji Medical College, Huazhong University of Science and Technology — Wuhan
Identifiers
NCT: NCT07620470 · 301168