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Clinical Trials/NCT06190821
NCT06190821RecruitingNot Applicable

Hydrodissection of the Hepatoduodenal Ligament

University Hospital, Strasbourg, France1 site in 1 country13 target enrollmentStarted: July 20, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Sponsor
Enrollment
13
Locations
1
Primary Endpoint
Retrospective description of the hepatoduodenal ligament dissection in the percutaneous treatment of liver lesions adjacent to the duodenum

Study Overview

Brief Summary

Percutaneous treatment of liver lesions adjacent to the duodenum exposes the duodenum to the risk of thermal injury, limiting removal and oncologic outcome. In this study the investigators investigate the feasibility of hepato duodenal ligament dissection in the percutaneous treatment of liver lesions adjacent to the duodenum.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Opposition to the reuse of his/her data for the purpose of scientific research.

Outcomes

Primary Outcomes

Retrospective description of the hepatoduodenal ligament dissection in the percutaneous treatment of liver lesions adjacent to the duodenum

Time Frame: Files analysed retrospectively from January 01, 2019 to July 31, 2022 will be examined

This study is retrospective

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University Hospital, Strasbourg, France
Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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