- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01551862
Complications in Lower Body Lifts
March 12, 2012 updated by: Dr. Hugo B. Kitzinger, Medical University of Vienna
Prospective Study on Complications Following a Lower Body Lift After Massive Weight Loss
A prospective study on 50 consecutive patients who are going to have a lower body lift procedure is performed.
Measures include comorbidities and complications.
Risk factors assessed including patient age, gender, highest lifetime body mass index (BMI) (BMI max), current BMI, excess weight loss (EWL), type of weight loss and nicotine consumption.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
50
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
-
-
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Vienna, Austria, 1090
- Medical University of Vienna, Dept. of Plastic Surgery
-
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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 64 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients which are referred to Department of Plastic Surgery for body contouring surgery
Description
Inclusion Criteria:
- after massive weight loss
- age > 18 years and < 65 years
- excess weight loss > 66%
- current body mass index < 35
- stable weight after weight loss for at least 12 months
Exclusion Criteria:
- insulin dependent diabetes mellitus
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Complications
Time Frame: 6 months
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Hugo B Kitzinger, MD, Medical University of Vienna
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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
January 1, 2007
Primary Completion (Actual)
March 1, 2011
Study Completion (Actual)
September 1, 2011
Study Registration Dates
First Submitted
March 6, 2012
First Submitted That Met QC Criteria
March 12, 2012
First Posted (Estimate)
March 13, 2012
Study Record Updates
Last Update Posted (Estimate)
March 13, 2012
Last Update Submitted That Met QC Criteria
March 12, 2012
Last Verified
March 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- PlastSurg01
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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