Korean OBEsity Surgical Treatment Study (KOBESS)
Primary Purpose
Bariatric Surgery Candidate, Obesity, Morbid
Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Sleeve gastrectomy or Roux-en-Y gastric bypass
Sponsored by
About this trial
This is an interventional treatment trial for Bariatric Surgery Candidate focused on measuring primary bariatric surgery, morbid obesity, South Korea, sleeve gastrectomy, Roux-en Y gastric bypass
Eligibility Criteria
Inclusion Criteria:
- body mass index (BMI) ≥ 35 kg/m2 or BMI ≥ 30 kg/m2 with co-morbidities such as hypertension, glucose intolerance, dyslipidemia, and sleep apnea
- being suitable for general anesthesia
- being able to give informed consent and committed to follow-up
- Female patients should have a negative urine pregnancy test at screening and agree to use reliable method of contraception for 1 year.
Exclusion Criteria:
- prior bariatric surgery of any kind
- being unable to understand the risks, benefits and compliance requirements of this trial
- pregnancy or planning on being pregnancy
- non-Korean speaker
- American society of anesthesiology (ASA) class IV or higher
- malignancy within 5 years.
Sites / Locations
- Seoul National University Bundang HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
bariatric surgery
Arm Description
This trial is a single-arm study and the enrolled patients are going to undergo sleeve gastrectomy (SG) or Roux-en-Y gastric bypass (RYGB). If the patient has Barrett's esophagus on the preoperative endoscopy, SG is not permitted. Inflammatory bowel disease and Helicobacter pylori infection on a rapid urease test are contraindications of RYGB.
Outcomes
Primary Outcome Measures
body weight (cm) change
waist circumference (cm) change
Secondary Outcome Measures
remission rates of obesity-related co-morbidity (hypertension, type 2 diabetes, dyslipidemia, and sleep apnea)
Quality of life change
EuroQol-5D (EQ-5D), the impact of weight on QoL (IWQOL) and the obesity-related psychosocial problem scale (OP-scale) are used to assess the improvement of QoL
Morbidity
Mortality
Micronutrients' deficiency
iron, ferritin, calcium, phosphate, albumin, vit.B12, vit.D, and parathyroid hormone
body composition change
bioelectrical impedance analysis and fat measurement CT
cost-effectiveness
cost-utility analysis using lifetime expected costs and quality-adjusted life years (QALYs)
Full Information
NCT ID
NCT03100292
First Posted
February 23, 2017
Last Updated
April 3, 2017
Sponsor
Seoul National University Bundang Hospital
Collaborators
Ministry of Health & Welfare, Korea
1. Study Identification
Unique Protocol Identification Number
NCT03100292
Brief Title
Korean OBEsity Surgical Treatment Study
Acronym
KOBESS
Official Title
Efficacy and Safety of Bariatric Surgery for Korean Morbidly Obese Patients : Prospective Multicenter Cohort Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2017
Overall Recruitment Status
Unknown status
Study Start Date
September 2016 (undefined)
Primary Completion Date
December 2017 (Anticipated)
Study Completion Date
December 2018 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Seoul National University Bundang Hospital
Collaborators
Ministry of Health & Welfare, Korea
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This trial is a multi-center, single-arm, prospective, observational cohort study of patients undergoing primary bariatric surgical procedures in Korea. A total of 100 patients will be recruited over a 1-year period from 2016 to 2017, and will be followed for a mean follow-up period of 1 year after surgery. The eligible subjects who have given their consent to participate will undergo one of two surgical procedures; sleeve gastrectomy and Roux-en Y gastric bypass.
The primary objective of this clinical trial is to measure the changes in body weight (kg) and waist circumference (cm) of the enrolled patients at postoperative 1 year. Secondary outcomes are improvement or remission rates of obesity-related co-morbidity (hypertension, type 2 diabetes, dyslipidemia, and sleep apnea), and the change in quality of life. Additionally, postoperative incidences of morbidity and mortality, micronutrient status, body composition, and cost-effectiveness of surgical intervention will be examined.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bariatric Surgery Candidate, Obesity, Morbid
Keywords
primary bariatric surgery, morbid obesity, South Korea, sleeve gastrectomy, Roux-en Y gastric bypass
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
100 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
bariatric surgery
Arm Type
Experimental
Arm Description
This trial is a single-arm study and the enrolled patients are going to undergo sleeve gastrectomy (SG) or Roux-en-Y gastric bypass (RYGB).
If the patient has Barrett's esophagus on the preoperative endoscopy, SG is not permitted. Inflammatory bowel disease and Helicobacter pylori infection on a rapid urease test are contraindications of RYGB.
Intervention Type
Other
Intervention Name(s)
Sleeve gastrectomy or Roux-en-Y gastric bypass
Primary Outcome Measure Information:
Title
body weight (cm) change
Time Frame
postoperative 1-year
Title
waist circumference (cm) change
Time Frame
postoperative 1-year
Secondary Outcome Measure Information:
Title
remission rates of obesity-related co-morbidity (hypertension, type 2 diabetes, dyslipidemia, and sleep apnea)
Time Frame
postoperative 1-year
Title
Quality of life change
Description
EuroQol-5D (EQ-5D), the impact of weight on QoL (IWQOL) and the obesity-related psychosocial problem scale (OP-scale) are used to assess the improvement of QoL
Time Frame
postoperative 1-year
Title
Morbidity
Time Frame
postoperative 1-year
Title
Mortality
Time Frame
postoperative 1-month
Title
Micronutrients' deficiency
Description
iron, ferritin, calcium, phosphate, albumin, vit.B12, vit.D, and parathyroid hormone
Time Frame
postoperative 1-year
Title
body composition change
Description
bioelectrical impedance analysis and fat measurement CT
Time Frame
postoperative 1-year
Title
cost-effectiveness
Description
cost-utility analysis using lifetime expected costs and quality-adjusted life years (QALYs)
Time Frame
postoperative 1-year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
body mass index (BMI) ≥ 35 kg/m2 or BMI ≥ 30 kg/m2 with co-morbidities such as hypertension, glucose intolerance, dyslipidemia, and sleep apnea
being suitable for general anesthesia
being able to give informed consent and committed to follow-up
Female patients should have a negative urine pregnancy test at screening and agree to use reliable method of contraception for 1 year.
Exclusion Criteria:
prior bariatric surgery of any kind
being unable to understand the risks, benefits and compliance requirements of this trial
pregnancy or planning on being pregnancy
non-Korean speaker
American society of anesthesiology (ASA) class IV or higher
malignancy within 5 years.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Young Suk Park, M.D.
Phone
+82-31-787-7099
Email
selteenzeus@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Do Joong Park, M.D., Ph.D.
Phone
+82-31-787-7099
Email
dojoongpark@gmail.com
Facility Information:
Facility Name
Seoul National University Bundang Hospital
City
Seongnam
State/Province
Gyeonggi-do
ZIP/Postal Code
13620
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Young Suk Park, M.D.
Phone
+82-31-787-7099
Email
selteenzeus@gmail.com
First Name & Middle Initial & Last Name & Degree
Do Joong Park, M.D., Ph.D.
Phone
+82-31-787-7099
Email
dojoongpark@gmail.com
First Name & Middle Initial & Last Name & Degree
Yoon-Seok Heo, M.D., Ph.D.
First Name & Middle Initial & Last Name & Degree
Hyuk-Joon Lee, M.D., Ph.D.
First Name & Middle Initial & Last Name & Degree
Sang-Moon Han, M.D., Ph.D.
First Name & Middle Initial & Last Name & Degree
Joo Ho Lee, M.D., Ph.D.
First Name & Middle Initial & Last Name & Degree
Sang-Uk Han, M.D., Ph.D.
First Name & Middle Initial & Last Name & Degree
Seung Wan Ryu, M.D., Ph.D.
First Name & Middle Initial & Last Name & Degree
Moon-Won Yoo, M.D., Ph.D.
First Name & Middle Initial & Last Name & Degree
Seung Ho Choi, M.D., Ph.D.
First Name & Middle Initial & Last Name & Degree
Tae Kyung Ha, M.D., Ph.D.
First Name & Middle Initial & Last Name & Degree
Sung-Soo Park, M.D., Ph.D.
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
34355282
Citation
Lee G, Park YS, Cho C, Lee H, Park J, Park DJ, Lee JH, Lee HJ, Ha TK, Kim YJ, Ryu SW, Han SM, Yoo MW, Park S, Han SU, Heo Y, Jung BH. Short-term changes in the serum metabolome after laparoscopic sleeve gastrectomy and Roux-en-Y gastric bypass. Metabolomics. 2021 Aug 5;17(8):71. doi: 10.1007/s11306-021-01826-y. Erratum In: Metabolomics. 2021 Sep 14;17(9):85.
Results Reference
derived
PubMed Identifier
29042391
Citation
Park YS, Park DJ, Lee JH, Lee HJ, Ha TK, Kim YJ, Ryu SW, Han SM, Yoo MW, Park S, Han SU, Heo Y. Korean OBEsity Surgical Treatment Study (KOBESS): protocol of a prospective multicentre cohort study on obese patients undergoing laparoscopic sleeve gastrectomy and Roux-en-Y gastric bypass. BMJ Open. 2017 Oct 16;7(10):e018044. doi: 10.1136/bmjopen-2017-018044.
Results Reference
derived
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Korean OBEsity Surgical Treatment Study
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