None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients who are referred to CT Brain, CECT Brain, CECT Thorax, and HRCT Thorax by the registered physician will be included in this study with valid informed consent and the procedure explained.
Exclusion criteria
Exclusion criteria: Patients who are un-cooperative, Patients who are allergic to contrast media, Patients with High BMI, Patients with high creatine and urea level.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To evaluate the radiation dose and image quality of 313 sample size which includes (CT Brain- 96, CECT Brain- 59, CECT Thorax - 72, HRCT Thorax - 86) standard dose and contrast volume protocol done with Iterative reconstruction algorithm for CT Brain Plain, CECT Brain, CECT Thorax and HRCT Thorax.Timepoint: 1 years from the date of starting the study | — |
Secondary
| Measure | Time frame |
|---|---|
| To compare the image quality & radiation dose of 313 samples which includes ( CT Brain- 96, CECT Brain - 59, CECT Thorax- 72, HRCT Thorax - 86)low dose & low contrast volume protocol with deep learning reconstruction algorithm with standard dose protocol iterative reconstruction algorithm for CT Brain Plain, CECT Brain, CECT Thorax & HRCT Thorax.Timepoint: 1 year from completion of Phase I. | — |
Countries
India
Contacts
Manipal College of Health Professions/Manipal Academy of Higher Education