- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05771259
Body Contouring After Bariatric Surgeries in Jordan
March 4, 2023 updated by: Amani Atallah, University of Jordan
Ody Contouring After Bariatric Surgeries in Jordan: Awareness, Prevalence, and Challenges
This study aimed to describe Jordanians' awareness and knowledge of body-contouring surgeries and estimate their prevalence.
Additionally, we aimed to identify the limitations reported by our population and compare them with those reported in the literature.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
We aimed to reach out to 351 patients who underwent bariatric surgery at JUH as well as an additional 100 patients who underwent BS at one of the largest private medical facilities in Amman between January and June of 2021.
We distributed a validated questionnaire to all patients.
Of the 451 patients, 305 completed the questionnaire (response rate: 67.6%).
The inclusion criteria were age 13-63 years, BS type (sleeve gastrectomy or Roux-en-Y bypass), and completion of the questionnaire.
Responses that did not meet these criteria or contained duplicates were excluded (n=11).
The remaining 294 responses were collected and entered into a database for the analysis.Three main variables were assessed in each group in addition to multiple other observations.
The main variables were sex, marital status, and employment status.
Study Type
Observational
Enrollment (Actual)
294
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
-
-
-
Amman, Jordan, 11942
- University of Jordan
-
-
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
13 years to 63 years (Child, Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Of the 451 patients, 305 completed the questionnaire (response rate: 67.6%).
The inclusion criteria were age 13-63 years, BS type (sleeve gastrectomy or Roux-en-Y bypass), and completion of the questionnaire.
Description
Inclusion Criteria:
- Age 13-63 years
- Bariatric surgery type (LSG or RYGB)
Exclusion Criteria:
- Incomplete or duplicate reponses
- Bariatric surgery ype (Gastric band)
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Group A
Participants who didn't undergo body contouring surgery after bariatric surgery.
|
Assessment of knowledge and behaviour
|
|
Group B
Participants who underwent body contouring surgery after bariatric surgery.
|
Assessment of knowledge and behaviour
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Prevalence of Body contouring surgeries after bariatric surgeries
Time Frame: 07/2017-06/2021
|
07/2017-06/2021
|
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.
General Publications
- Nguyen NT, Root J, Zainabadi K, Sabio A, Chalifoux S, Stevens CM, Mavandadi S, Longoria M, Wilson SE. Accelerated growth of bariatric surgery with the introduction of minimally invasive surgery. Arch Surg. 2005 Dec;140(12):1198-202; discussion 1203. doi: 10.1001/archsurg.140.12.1198.
- Ellison JM, Steffen KJ, Sarwer DB. Body Contouring After Bariatric Surgery. Eur Eat Disord Rev. 2015 Nov;23(6):479-87. doi: 10.1002/erv.2408. Epub 2015 Sep 22.
- Monpellier VM, Antoniou EE, Mulkens S, Janssen IMC, Jansen ATM, Mink van der Molen AB. Body Contouring Surgery after Massive Weight Loss: Excess Skin, Body Satisfaction, and Qualification for Reimbursement in a Dutch Post-Bariatric Surgery Population. Plast Reconstr Surg. 2019 May;143(5):1353-1360. doi: 10.1097/PRS.0000000000005525.
- Derderian SC, Patten L, Kaizer AM, Inge TH, Jenkins TM, Michalsky MP, Xie C, Dewberry LC, Sitzman TJ. Body contouring in adolescents after bariatric surgery. Surg Obes Relat Dis. 2020 Jan;16(1):137-142. doi: 10.1016/j.soard.2019.09.063. Epub 2019 Sep 18.
- Aldaqal SM, Samargandi OA, El-Deek BS, Awan BA, Ashy AA, Kensarah AA. Prevalence and desire for body contouring surgery in postbariatric patients in saudi arabia. N Am J Med Sci. 2012 Feb;4(2):94-8. doi: 10.4103/1947-2714.93386.
- Hult M, Bonn SE, Brandt L, Wiren M, Lagerros YT. Women's Satisfaction with and Reasons to Seek Bariatric Surgery-a Prospective Study in Sweden with 1-Year Follow-up. Obes Surg. 2019 Jul;29(7):2059-2070. doi: 10.1007/s11695-019-03834-3.
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 (Actual)
July 1, 2017
Primary Completion (Actual)
June 30, 2021
Study Completion (Actual)
February 20, 2023
Study Registration Dates
First Submitted
March 4, 2023
First Submitted That Met QC Criteria
March 4, 2023
First Posted (Actual)
March 16, 2023
Study Record Updates
Last Update Posted (Actual)
March 16, 2023
Last Update Submitted That Met QC Criteria
March 4, 2023
Last Verified
March 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 10/2023/5723
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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