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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01801514
Other study ID # iCT DL
Secondary ID
Status Completed
Phase N/A
First received February 27, 2013
Last updated November 10, 2014
Start date November 2012
Est. completion date March 2014

Study information

Verified date November 2014
Source Philips Healthcare
Contact n/a
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Interventional

Clinical Trial 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


Recruitment information / eligibility

Status Completed
Enrollment 337
Est. completion date March 2014
Est. primary completion date March 2014
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

1. Male or female subject

2. Subjects with relative clinical findings indicative for CT examination. CT referral request approved by a physician is needed

3. Voluntary signed the Informed Consent Form

Exclusion Criteria:

1. Pregnant or potentially pregnant female subjects

2. Subjects who are not able or not willing to give written Informed Consent without a caregiver consent

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic


Related Conditions & MeSH terms

  • Other Conditions That May Be A Focus of Clinical Attention

Intervention

Device:
Computed Tomography scan
Routine Computed Tomography scan

Locations

Country Name City State
Israel Hadassah-Hebrew University Medical Center Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Philips Healthcare

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Capability of producing dual energy computed tomography imaging and dual energy applications 6 months No
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