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Clinical Trials/NCT02655094
NCT02655094CompletedNot Applicable

Unilateral Pulmonary Edema After Minimal-invasive Mitral Valve Surgery: a Retrospective Single Center Observation

University Hospital Schleswig-Holstein1 site in 1 country256 target enrollmentStarted: February 2016Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
256
Locations
1
Primary Endpoint
Unilateral right sided pulmonary edema or congestion after surgery

Study Overview

Brief Summary

Unilateral pulmonary edema after minimal-invasive mitral valve surgery is a rare but in some cases severe complications, sometimes causing extracorporeal life support. The investigators have observed over several years 5 cases of instantaneous postoperative severe pulmonary edema. This is a retrospective analysis of over 200 minimal-invasive mitral valve surgery procedure.

Detailed Description

Unilateral pulmonary edema after minimal-invasive mitral valve surgery is a rare but in some cases severe complications, sometimes causing extracorporeal life support. The investigators have observed over several years 5 cases of instantaneous postoperative severe pulmonary edema. After having studied the available literature on this particular topic the investigators have decided to prepare a retrospective analysis of over 200 minimal-invasive mitral valve surgery procedure focusing on radiological and clinical signs of unilateral pulmonary edema.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to 99 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • >= 18 years of age

Exclusion Criteria

  • urgent surgery

Outcomes

Primary Outcomes

Unilateral right sided pulmonary edema or congestion after surgery

Time Frame: Postoperatively within the first 12h after admission to intensive care unit

retrospective analysis using the electronic and the paper-based patient specific database

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
University Hospital Schleswig-Holstein
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Dr. Jochen Renner

PD Dr.

University Hospital Schleswig-Holstein

Study Sites (1)

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