- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05054972
Left Renal Vein Division for Juxtarenal Aortic Exposure
September 19, 2021 updated by: Dr. Andreas Selberherr, Medical University of Vienna
Left Renal Vein Division for Juxtarenal Aortic Exposure: Renal Function and Role of the Communicating Lumbar Vein
Retrospective study on the outcome of the renal function in patients operated because of juxtarenal aortic aneurysms.
Study Overview
Status
Active, not recruiting
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
110
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Vienna, Austria
- Department of Vascular Surgery, Medical University of Vienna
-
-
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
18 years to 100 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients who were treated surgically for a juxtrarenal aortic aneurysm with an open operation.
Description
Inclusion Criteria:
Only patients who went for a planned operation because of a juxtarenal aortic aneurysm were included in this retrospective analysis.
Exclusion Criteria:
Emergency surgery Rupture Pending rupture
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 |
---|---|
A
Group of patients in whom the left renal vein was divided for exposure of the aorta.
|
Surgical procedure in which an aortic aneurysm is excluded.
|
A+
Subgroup of group A in whom a communicating vein to the left ascending lumbar vein was present.
|
Surgical procedure in which an aortic aneurysm is excluded.
|
A-
Subgroup of group A in whom a communicating vein to the left ascending lumbar vein was not present.
|
Surgical procedure in which an aortic aneurysm is excluded.
|
B
Group of patients in whom the left renal vein was mobilized but not divided for exposure of the aorta.
|
Surgical procedure in which an aortic aneurysm is excluded.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Renal function after surgery.
Time Frame: 24 months
|
The level of creatinine in the blood was measured after surgery at several time points.
|
24 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
October 1, 2020
Primary Completion (Anticipated)
December 30, 2021
Study Completion (Anticipated)
December 30, 2021
Study Registration Dates
First Submitted
September 19, 2021
First Submitted That Met QC Criteria
September 19, 2021
First Posted (Actual)
September 23, 2021
Study Record Updates
Last Update Posted (Actual)
September 23, 2021
Last Update Submitted That Met QC Criteria
September 19, 2021
Last Verified
September 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- ComLum
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
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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