N/A
N=49
Clinical Evaluation for General Electric (GE) CT System
CT Scanners X Ray
Bottom Line
View on ClinicalTrials.gov: NCT01909180 ↗Enrolled (actual)
49
Serious AEs
0.0%
Results posted
Apr 2016
Primary outcome: Primary: Image Quality — 4.53; 4.44; 4.63 units on a scale
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Revolution CT Scanner (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- GE Healthcare
- Primary completion
- Nov 2013
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Image Quality |
4.53; 4.44; 4.63 | — |
Summary
An external evaluation to obtain clinical data to create sample clinical images.
The data will also be used for product and technology development, marketing materials, and inclusion in publications.
Eligibility Criteria
Inclusion Criteria
- Subjects who voluntarily signed the Informed Consent Form (ICF).
- Male subjects 18 years of age or older.
- Female subjects 18 years of age or older. Females between 18 and 60 years of age must be non-lactating and non-pregnant as confirmed by negative urine pregnancy test., unless they had surgery resulting in sterilization or are post-menopausal according to the medical history.
Exclusion Criteria
- • Subjects previously enrolled in this Evaluation.
- Subjects who are not able or not willing to give written Informed Consent.
- For IV contrast-enhanced CT exams, anyone with known or suspected allergy to iodinated contrast agents or a history of multiple allergies or asthma.
- For IV contrast-enhanced CT exams, per the institution's guidelines on risk stratification and prophylaxis for Contrast Induced Neuropathy, subjects will be pre-screened via medical history review by qualified medical personnel for suspected renal function impairment and high risk subjects will undergo a serum creatinine lab test. Any subject with proven renal insufficiency will be excluded.
- Known pregnancy and nursing (lactating) females.
- Any subject with urgent medical condition requiring acute care.
- Any conditions that, in the opinion of the Investigator, would interfere with the evaluation of the results or constitute a health hazard for the subject.
- Subjects who do not agree to allow GEHC personnel to be present during the scan.
Data sourced from ClinicalTrials.gov (NCT01909180). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.