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

Study Type

Observational

Enrollment (Estimated)

10

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • Saint-Priest-en-Jarez, France, 42270
        • Recruiting
        • CHU de Saint-Etienne
        • Sub-Investigator:
          • Rémi Grange, MD
        • Principal Investigator:
          • Sylvain Grange, MD
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patients with interrupted IVC with azygous continuation on CT scan

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Sylvain GRANGE, MD, CHU de Saint-Etienne

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2024

Primary Completion (Estimated)

March 31, 2024

Study Completion (Estimated)

March 31, 2024

Study Registration Dates

First Submitted

March 4, 2024

First Submitted That Met QC Criteria

March 8, 2024

First Posted (Actual)

March 15, 2024

Study Record Updates

Last Update Posted (Actual)

March 15, 2024

Last Update Submitted That Met QC Criteria

March 8, 2024

Last Verified

February 1, 2024

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)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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