CT 5400 RT System Application Clinical Study

Philips

Status

Completed

Conditions

Computed Tomography Workflow Assessment

Treatments

Radiation: Computed Tomography

Study type

Interventional

Funder types

Industry

Identifiers

NCT06595888

300200

Details and patient eligibility

About

The purpose of this study is to assess the satisfaction of the common functions, the operation convenience, and the whole system stability, and the safety of CT 5400 RT System.

Enrollment

190 patients

Sex

All

Ages

18 to 75 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

18≤ Age ≤ 75 years old
Subjects with Clear consciousness; Subjects can cooperate and act autonomously
Subjects agree to participate in this clinical study and sign the subject's informed consent
Women subjects of childbearing age should have a negative pregnancy test and should have no plans to become pregnant in the next 6 months

Exclusion criteria

Subjects who do not have full capacity for civil conduct;
Women subjects who are pregnant or in lactating phase;
Subjects who have had a CT scan within one year;
Subjects with a history of allergies or asthma, severe hepatic and renal insufficiency or hyperthyroidism in which are considered as contraindication for CT contrast-enhanced examination;
According to the opinion of the investigator: any situation that may affect the evaluation of the results or expose subjects into health risk;
Subjects with mental disorders who cannot cooperate with the examination