MR Quality + Diagnostic Performance for CHC Diagnosis - Gadoxetic Acid, Gadoteric Acid and P03277 Comparison
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| ClinicalTrials.gov Identifier: NCT04652947 |
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Recruitment Status :
Completed
First Posted : December 3, 2020
Last Update Posted : December 3, 2020
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Sponsor:
University Hospital, Angers
Information provided by (Responsible Party):
University Hospital, Angers
- Study Details
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Brief Summary:
Compare diagnostic MRI performance of gadoteric acid, gadoxetic acid and P03277 for suspected CHC nodules less than 3 cm, using LIRADS criteria
| Condition or disease | Intervention/treatment |
|---|---|
| Hepatocellular Carcinoma | Diagnostic Test: MRI diagnostic |
| Study Type : | Observational |
| Actual Enrollment : | 30 participants |
| Observational Model: | Cohort |
| Time Perspective: | Retrospective |
| Official Title: | MR Quality + Diagnostic Performance for CHC Diagnosis - Gadoxetic Acid, Gadoteric Acid and P03277 Comparison |
| Actual Study Start Date : | December 7, 2016 |
| Actual Primary Completion Date : | October 26, 2017 |
| Actual Study Completion Date : | October 26, 2017 |
Intervention Details:
- Diagnostic Test: MRI diagnostic
no intervention, patient only have MRI
Primary Outcome Measures :
- compare diagnostic MRI performance of gadoteric acid, gadoxetic acid and P03277 for suspected CHC nodules [ Time Frame: 3 months ]the evaluation criteria will be the classification of each nodule according to the LiRADS citeria
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| Ages Eligible for Study: | 18 Years and older (Adult, Older Adult) |
| Sexes Eligible for Study: | All |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Patients followed for hepatopathy
Criteria
Inclusion Criteria:
- Patients who had all three MRI scans as part of the diagnosis of the same suspected CHC lesion(s)
- Reference diagnosis obtained for suspected CHC nodules by a diagnostic algorithm taking into account histology, imaging and follow-up
Exclusion Criteria:
- Delay between first MRI and 3rd MRI greater than 3 months
No Contacts or Locations Provided
| Responsible Party: | University Hospital, Angers |
| ClinicalTrials.gov Identifier: | NCT04652947 |
| Other Study ID Numbers: |
2018-74 |
| First Posted: | December 3, 2020 Key Record Dates |
| Last Update Posted: | December 3, 2020 |
| Last Verified: | July 2020 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
Additional relevant MeSH terms:
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Carcinoma, Hepatocellular Adenocarcinoma Carcinoma Neoplasms, Glandular and Epithelial Neoplasms by Histologic Type Neoplasms |
Liver Neoplasms Digestive System Neoplasms Neoplasms by Site Digestive System Diseases Liver Diseases |

