CompletedNot Applicable

Applications of Dual-Energy Computed Tomography

Israel337 participantsStarted 2012-11

Plain-language summary

The purpose of the study is to evaluate the feasibility of multilayer detection-based dual energy computed tomography scanner and to assess the added diagnostic value of dual energy applications

Who can participate

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Male or female subject
. Subjects with relative clinical findings indicative for CT examination. CT referral request approved by a physician is needed
. Voluntary signed the Informed Consent Form

Exclusion criteria

. Pregnant or potentially pregnant female subjects
. Subjects who are not able or not willing to give written Informed Consent without a caregiver consent

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Capability of producing dual energy computed tomography imaging and dual energy applications

Timeframe: 6 months

Trial details

NCT IDNCT01801514

SponsorPhilips Healthcare

Sponsor typeINDUSTRY

Study typeINTERVENTIONAL

Primary completion2014-03

View on ClinicalTrials.gov More Other Conditions That May Be A Focus of Clinical Attention trials

Who can participate

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Male or female subject
. Subjects with relative clinical findings indicative for CT examination. CT referral request approved by a physician is needed
. Voluntary signed the Informed Consent Form

Exclusion criteria

. Pregnant or potentially pregnant female subjects
. Subjects who are not able or not willing to give written Informed Consent without a caregiver consent