- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02151799
The Effects of Body Contouring: Abdominoplasty and Liposuction
November 3, 2015 updated by: Tampere University Hospital
Body Contouring - the Analysis of Non-invasive and Invasive Methods and Their Interventional Effects on Quality of Life
The data regarding the effects of aesthetic body contouring is insufficient.
Poor results may related to preoperative psychological distress.
Studies regarding eating disorder symptoms are lacking.
Therefore studies using standardized and validated are needed.
We decided to prospectively study quality of life, psychological distress, and eating disorder symptoms in body contouring (abdominoplasty or liposuction) patient populations.
Used questionnaires are 15D quality of life, Raitasalo's modification of the Beck Inventory, and the Eating Disorder Inventory.
We hypothesize that aesthetic body contouring plastic surgery has notable quality of life effects.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
143
Phase
- Phase 4
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 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- patients requesting body contouring surgery
Exclusion Criteria:
- previous abdominal aesthetic surgery, simultaneous other aesthetic surgery at the same time
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
- Primary Purpose: TREATMENT
- Allocation: NA
- Interventional Model: SINGLE_GROUP
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Body contouring surgery
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Quality of life
Time Frame: 6 months
|
15D quality of life questionnaire RBDI mood questionnaire Eating Disorder Inventory questionnaire
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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.
Helpful Links
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, 2010
Primary Completion (Actual)
February 1, 2014
Study Completion (Actual)
November 1, 2015
Study Registration Dates
First Submitted
May 28, 2014
First Submitted That Met QC Criteria
May 28, 2014
First Posted (Estimate)
May 30, 2014
Study Record Updates
Last Update Posted (Estimate)
November 4, 2015
Last Update Submitted That Met QC Criteria
November 3, 2015
Last Verified
November 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- R09166
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.
Clinical Trials on Subcutaneous Abdominal Fat
-
CAO Group, Inc.CompletedAbdominal Subcutaneous FatUnited States
-
BodyAesthetic Research CenterCompletedAbdominal Subcutaneous FatUnited States
-
Asklepios proresearchEthicon Endo-SurgeryCompleted
-
Biopolis S.L.University Rovira i Virgili; Hospital Universitari Sant Joan de Reus; Technological...UnknownObesity | Intra-Abdominal Fat | Subcutaneous Fat, AbdominalSpain
-
Caliway Biopharmaceuticals Co., Ltd.RecruitingSubcutaneous FatUnited States
-
Caliway Biopharmaceuticals Co., Ltd.Active, not recruitingSubcutaneous FatUnited States
-
Caliway Biopharmaceuticals Co., Ltd.CompletedSubcutaneous FatUnited States
-
Caliway Biopharmaceuticals Co., Ltd.Completed
-
Cynosure, Inc.Completed
-
Northwestern UniversityCompleted
Clinical Trials on Abdominoplasty and liposuction
-
Karolinska University HospitalWithdrawn
-
Federal University of São PauloUnknown
-
Mansoura UniversityCompleted
-
Federal University of São PauloCompleted
-
Loma Linda UniversityWithdrawn
-
AntriaCompletedSoft Tissue Mass RemovalUnited States
-
Assiut UniversityUnknown
-
Lille Catholic UniversityNot yet recruitingHidradenitis SuppurativaFrance
-
University of AarhusCompletedMesenchymal Stem Cells
-
Assiut UniversityRecruitingAbdomen EnlargedEgypt