Natural History of Asymptomatic Superior Mesenteric Arterial Stenosis.

Sponsor
Hospices Civils de Lyon (Other)
Overall Status
Completed
CT.gov ID
NCT04785105
Collaborator
(none)
77
1
36.9
2.1

Study Details

Study Description

Brief Summary

The aim of this study was to evaluate asymptomatic superior mesenteric artery (SMA) stenosis prognosis according to the presence of coeliac artery (CA) and/or inferior mesenteric artery (IMA) associated stenosis.

Condition or Disease Intervention/Treatment Phase
  • Other: No intervention

Detailed Description

BACKGROUND: The benefit of preventive treatment for SMA stenosis remains uncertain. The latest guidelines remain unclear given the lack of data in the literature.

Study Design

Study Type:
Observational
Actual Enrollment :
77 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Natural History of Asymptomatic Superior Mesenteric Arterial Stenosis Depends on Celiac and Inferior Mesenteric Arteries Status.
Actual Study Start Date :
Feb 1, 2017
Actual Primary Completion Date :
Dec 1, 2019
Actual Study Completion Date :
Mar 1, 2020

Arms and Interventions

Arm Intervention/Treatment
patient with isolated SMA stenosis

patient with isolated SMA stenosis on initial scanner

Other: No intervention
No intervention

patient with both SMA stenosis and CA or/and IMA stenosis

patient with both SMA stenosis and CA or/and IMA stenosis on initial scanner

Other: No intervention
No intervention

Outcome Measures

Primary Outcome Measures

  1. Development of mesenteric disease defined as acute mesenteric ischemia or chronic mesenteric ischemia. [4 years]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • the presence of coeliac artery (CA) and/or inferior mesenteric artery (IMA) associated stenosis.
Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Groupement Hospitalier Est Bron France 69500

Sponsors and Collaborators

  • Hospices Civils de Lyon

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hospices Civils de Lyon
ClinicalTrials.gov Identifier:
NCT04785105
Other Study ID Numbers:
  • SMA_2020
First Posted:
Mar 5, 2021
Last Update Posted:
Mar 5, 2021
Last Verified:
Jun 1, 2020
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hospices Civils de Lyon
Additional relevant MeSH terms:

Study Results

No Results Posted as of Mar 5, 2021