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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT02076737
Date of registration: 21/02/2014
Prospective Registration: No
Primary sponsor: University Hospital, Clermont-Ferrand
Public title: Model-based Iterative Reconstruction (MB-IR VEOTM) in Ultra Low-dose Abdominal CT Versus Adaptative Statistical Iterative Reconstruction (ASIR): A Prospective Study for Acute Renal Colic VEOLITH
Scientific title: Model-based Iterative Reconstruction (MB-IR VEOTM) in Ultra Low-dose Abdominal CT Versus Adaptative Statistical Iterative Reconstruction (ASIR): A Prospective Study for Acute Renal Colic
Date of first enrolment: February 2013
Target sample size: 120
Recruitment status: Completed
URL:  http://clinicaltrials.gov/show/NCT02076737
Study type:  Interventional
Study design:  Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic  
Phase:  N/A
Countries of recruitment
France
Contacts
Name:     Louis BOYER
Address: 
Telephone:
Email:
Affiliation:  University Hospital, Clermont-Ferrand
Key inclusion & exclusion criteria

Inclusion Criteria:

- Informed and a written consent

- Acute flank pain needed abdominal CT exploration.

Exclusion Criteria:

- Juvenile patients

- Pregnant women



Age minimum: 18 Years
Age maximum: 90 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Model-based Iterative Reconstruction (MB-IR VEOTM)
Intervention(s)
Device: Model-based iterative reconstruction (MB-IR VEOTM) on CT Discovery 750HD (GE Healthcare, Milwaukee, WI)
Primary Outcome(s)
acute renal colic [Time Frame: at day 1]
Secondary Outcome(s)
Measurements of subjective image quality [Time Frame: at day 1]
Measure of dose-length product [Time Frame: at day 1]
Evaluation of visceral fat [Time Frame: at ady 1]
Secondary ID(s)
CHU-0183
2012-A01699-34
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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