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Comparative Analysis Between Sleeve Gastrectomy and Roux-en Y Gastric Bypass in Bariatric Operation

Not Applicable
Conditions
Overnutrition
Overweight and Obesity
Obesity, Morbid
Nutrition Disorders
Body Weight Changes
Interventions
Procedure: Roux-en-Y gastric bypass
Procedure: Sleeve gastrectomy
Registration Number
NCT04554758
Lead Sponsor
Inha University Hospital
Brief Summary

Prospective, double-arm, multi-center cohort study on obese patients, for laparoscopic sleeve gastrectomy versus Roux-en Y gastric bypass

Detailed Description

This is prospective cohort study. Total 400 obese patients will be enrolled(Sleeve gastrectomy 200 patients, Roux-en-Y gastric bypass 200)

The principal investigator or another clinical investigator in charge will individually inform the patients about the study, before operation at out patient clinic. At that time patient is selected to either sleeve gastrectomy group or Roux-en-Y gastric bypass group. All investigator report to clinical research center about patients BMI and operation method.

About 30-35 obesity patients will be enrolled according to their BMI status. Patients' BMI status is classified into several parts by 2.5 gap started from 27.5.

All patients will undergo periodically anthropometry, laboratory tests, bioelectrical impedance analysis, gastrofiberscopy, polysomnography and abdomen CT before and after surgery.

Patients with hypertension will undergo echocardiography. Patients with polycystic ovary syndrome will be checked hormonal study. Patients with type 2 diabetes mellitus will be performed 75g oral glucose tolerance test test.

Surgical complication include wound morbidities, gastrointestinal leakage or fistula, postoperative bleeding, intra-abdominal abscess, stricture , adhesive ileus, reflux esophagitis, marginal ulceration, dumping syndrome and internal hernia.

Systemic complication which is not associated with the operation field include ling morbidities, heart morbidities, urinary morbidities and others.

Hospital mortality is defined as postoperative death form any cause within 30 days after operation.

All patients will be followed up post operative 1 month, 3 month, 6 month, 12 month, 18 month, 24 month.

All patients' liver tissue, visceral fat and subcutaneous fat will be harvested during operation.

All patients' blood sample will be collected at out patient clinic visit. All patients' urine and face will be collected at out patient clinic visit and will be analyzed to evaluate microbial change throughout pre and post operation period.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
400
Inclusion Criteria
  • obesity patients(BMI over 35)
  • morbid obesity patients(BMI over 30) with cardiovascular disease, hypertension, hyperlipidemia, type 2 diabetes mellitus, obstructive sleep apnea
  • type 2 diabetes mellitus obesity patients(BMI over 27.5) who were treated medical therapy or HbA1C level over 7%
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Exclusion Criteria
  • Patients who underwent previously bariatric operation
  • Patients who were diagnosed malignant disease patients within 5 years
  • Patients who were involved with other clinical trial within 3 months
  • Patients who are risky to conduct general anesthesia for operation
Read More

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Roux-en-Y gastric bypassRoux-en-Y gastric bypass200 obesity patients who undergo laparoscopic Roux-en-Y gastric bypass
Sleeve gastrectomySleeve gastrectomy200 obesity patients who undergo laparoscopic sleeve gastrectomy
Primary Outcome Measures
NameTimeMethod
Body weight change ratePostoperative 1 year

Decreased body weight proportion compare to preoperative body weight

Obesity Cure Success RatePostoperative 1 year

Proportion of patients who reach BMI bellow 25

Waist circumference change ratePostoperative 1 year

Decreased waist circumference change proportion compare to preoperative waist circumference

Secondary Outcome Measures
NameTimeMethod
Quality of life improvement rate and degree-2Postoperative 1 year, 2 year

EQ-VAS(EuroQol-Visual Analogue scale) is a question scale ranging form 0 to 100.

0 indicated the worst and 100 indicated the best condition. EQ-VAS provides important, complementary information on patient's view about their own health.

Postoperative complication rate and mortality rateWithin postoperative 30 days

Number of participants surgical complications associate with the surgical technique or the operation field Number of participants mortality after operation associated with surgical complication or underlying disease

Quality of life improvement rate and degree-4Postoperative 1 year, 2 year

Moore-head-Ardelt QoL questionnaire II(MA-II) has 6 items(general self-esteem, physical activity, social contacts, satisfaction concerning work, pleasure related to sexuality and focus on eating behavior).

All items are scored according to 10-level Likert scale(-0.5 to 0.5) and all have the same weight.

Quality of life improvement rate and degree-3Postoperative 1 year, 2 year

Impact of Weight on QoL(IWQoL) has 5 dimensions and each dimension has several items.

* physical function : 11 items

* self-esteem : 7 items

* sexual life : 4 items

* public distress : 5 items

* work : 4 items

Score range from 0 to 100 and 100 represents the best quality of life.

Quality of life improvement rate and degree-1Postoperative 1 year, 2 year

Patients rate and quantitative analysis of the improved life quality using several survey EQ-5D-3L(EuroQol-5D) consists of 5 dimensions(mobility, self-care, usual activities, pain/discomfort and anxiety/depression).

Each of which is scored as no/some/extreme problems. The dimension scores are converted into health utility scores ranging form 0(death) to 1(perfect health)

Rate of morbid disease remission or partial remissionPostoperative 1 year, 2 year

Remission rate or partial remission rate of morbid disease related to obesity such as hypertension, type 2 diabetes mellitus, hyperlipidemia after surgery

Micronutrient deficiencyPostoperative 1 year, 2 year

Incidence of micronutrient deficiency rate such as vitamine, calcium, iron

Quality of life improvement rate and degree-5Postoperative 1 year, 2 year

Obesity-related Psychosocial Problem scale(OP scale) consists of 8 items that measure the bothersome impact of body weight on given situations.

(private gatherings in their own home, private gatherings at their friend or relative's home and going to restaurant)

Trial Locations

Locations (1)

Inha University Hospital

🇰🇷

Incheon, Korea, Republic of

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