- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06312878
CT Features of Interrupted Inferior Vena Cava With Azygous Continuation
CT Features of Interrupted Inferior Vena Cava With Azygous Continuation : a Retrospective Study
Inferior vena cava (IVC) is the largest vein is the body, draining blood from the abdomen, pelvis and lower extremities. IVC anomalies can be congenital or acquired.
The origins of these anomalies are not entirely clear, and their incidence is uncertain.
Imaging plays a pivotal role in diagnosis to prevent misinterpretation. CT scan is a quick, available, and suitable imaging modality in emergency setting.
The aim of this retrospective monocentric study was of describe CT features of interrupted suprarenal inferior vena cava with azygous continuation.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Rémi GRANGE, MD
- Phone Number: +33 (0)477828963
- Email: remi.grange@chu-st-etienne.fr
Study Contact Backup
- Name: Sylvain Grange, MD
- Phone Number: +33 (0)477829066
- Email: grangesylvain@hotmail.fr
Study Locations
-
-
-
Saint-Priest-en-Jarez, France, 42270
- Recruiting
- CHU de Saint-Etienne
-
Sub-Investigator:
- Rémi Grange, MD
-
Principal Investigator:
- Sylvain Grange, MD
-
Contact:
- Sylvain Grange, MD
- Phone Number: +33 (0)477829066
- Email: grangesylvain@hotmail.fr
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- All patients with interrupted IVC with azygous continuation on CT scan were included in this study.
Exclusion Criteria:
- Patients under 18 years of age
- Patients no available CT scan.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Included patients
All patients with interrupted IVC with azygous continuation on CT scan.
|
Evaluated technique by collecting data from the medical record.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Describe CT features of interrupted suprarenal inferior vena cava with azygous continuation
Time Frame: Day : 1
|
The number of infrarenal inferior vena cava was recorded for each patient.
|
Day : 1
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Describe CT features of interrupted suprarenal inferior vena cava with azygous continuation
Time Frame: Day : 1
|
The type of drainage of the left renal vein was recorded for each patient.
|
Day : 1
|
Describe association with polysplenic syndrome
Time Frame: Day : 1
|
Measurement of splenic laterality
|
Day : 1
|
Describe association with polysplenic syndrome
Time Frame: Day : 1
|
Measurement of stomach laterality
|
Day : 1
|
Describe association with polysplenic syndrome
Time Frame: Day : 1
|
Measurement of liver morphology
|
Day : 1
|
Describe association with polysplenic syndrome
Time Frame: Day : 1
|
Measurement of the preduodenal portal vein
|
Day : 1
|
Describe association with polysplenic syndrome
Time Frame: Day : 1
|
Measurement of pancreatic and intestinal rotation malformations
|
Day : 1
|
Describe association with polysplenic syndrome
Time Frame: Day : 1
|
Measurement of cardiopulmonary malformations
|
Day : 1
|
Describe circumstances of discovering the interrupted IVC
Time Frame: Day : 1
|
The circumstances of discovering the interrupted IVC were also documented from clinical records.
|
Day : 1
|
Describe circumstances of discovering the interrupted IVC
Time Frame: Day : 1
|
An history of thrombotic events was also documented from clinical records.
|
Day : 1
|
Collaborators and Investigators
Investigators
- Principal Investigator: Sylvain GRANGE, MD, CHU de Saint-Etienne
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- IRBN052024/CHUSTE
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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