Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
50 participants
INTERVENTIONAL
2018-11-19
2021-11-18
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Bariatric surgery patients
Bariatric patients undergoing sleeve gastrectomy or Roux-en-Y gastric bypass
Bariatric surgery
Bariatric surgery including sleeve gastrectomy and Roux-en-Y gastric bypass
Interventions
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Bariatric surgery
Bariatric surgery including sleeve gastrectomy and Roux-en-Y gastric bypass
Eligibility Criteria
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Inclusion Criteria
* body mass index ≥27.5 kg/m2, in case of type 2 diabetes
* body mass index ≥35 kg/m2, in case of non-type 2 diabetes
Exclusion Criteria
* Abdominal, thoracic, pelvic, and/or obstetric-gynecologic surgery within 3 months or at the discretion of the Investigator
* Cardiovascular conditions including significant known coronary artery disease (CAD), uncompensated congestive heart failure, history of stroke, or uncontrolled hypertension (defined as medially treated with the mean of three separate measurements systolic blood pressure \>180 mmHg or diastolic blood pressure \>110 mmHg).
Subjects with CAD who were successfully treated with coronary artery bypass graft or percutaneous coronary intervention within 3 months and who have no evidence of active ischemia are eligible
* Kidney diseases including renovascular hypertension, renal artery stenosis, or end-stage renal disease
* Known history of chronic liver diseases including liver cirrhosis and alpha-1-antitrypsin deficiency
* Gastrointestinal disorders including a known history of celiac disease or any other malabsorptive disorders or inflammatory bowel disease (Crohn's disease or ulcerative colitis)
* Psychiatric disorders including dementia, active psychosis, history of suicide attempts, and alcohol or drug abuse within 12 months
* Severe pulmonary disease defined as forced expiratory volume at one second \<50% of the predicted value
* Anemia defined as hemoglobin \<8 in females and 10 in males
* Malignancy within 5 years (except squamous cell and basal cell cancer of the skin). Subjects diagnosed with early or stage 1 cancer that was successfully treated are eligible based on the Investigator's discretion
* Any condition or major illness that in the Investigator's judgement places the subject at undue risk by participating in the study
* Pregnancy
* Unable to understand the risks, realistic benefits, and compliance requirements of each program
* Use of investigational therapy or participation in any other clinical trial within 3 months
* Plans to move outside South Korea within the next 2 years
19 Years
ALL
No
Sponsors
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Korea University Anam Hospital
OTHER
Responsible Party
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Sungsoo Park
Professor
Principal Investigators
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Sungsoo Park, MD,PhD
Role: PRINCIPAL_INVESTIGATOR
Korea University
Locations
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Korea University Anam Hospital
Seoul, , South Korea
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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STARDOM-Bari
Identifier Type: -
Identifier Source: org_study_id
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