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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02406664
Other study ID # NCT02271568
Secondary ID
Status Recruiting
Phase N/A
First received March 19, 2015
Last updated February 18, 2016
Start date January 2015
Est. completion date December 2017

Study information

Verified date February 2016
Source Hanyang University
Contact Tae Kyung Ha, MD,PhD
Phone 82-2-2290-8444
Email missurgeon@hanyang.ac.kr
Is FDA regulated No
Health authority Korea: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the change in kidney function and blood pressure after gastric bypass versus conventional medical therapy in morbid obesity. The study mainly focus on glomerular filtration rate(GFR) with known relation to the renal function and 24 hours ambulatory blood pressure monitoring after intervention of gastric bypass or medical treatment.


Description:

Metabolic syndrome is strongly associated with obesity and the patients with this syndrome are at increased risk for cardiovascular disease. Obesity constitutes a strong risk factor for the development of chronic kidney disease. Among diabetics, obesity is known to amplify the risk for kidney disease. Bariatric surgery has yielded dramatic results including longitudinal loss of excess body weight and either complete reversal or significant improvement of several features of metabolic syndrome. In addition, many observational studies have demonstrated significant reduction in proteinuria after bariatric surgery.

However, the changes in the component of cardiovascular problem among metabolic syndrome and changes in renal filtration function or progression to end stage kidney disease in morbidly obese patients after weight loss surgery have not been extensively studied. Therefore, our study mainly focus on glomerular filtration rate(GFR) with known relation to the renal function and 24 hours ambulatory blood pressure monitoring after intervention of gastric bypass or medical treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date December 2017
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Morbid obesity (BMI>30) patients with one of comorbidity (type 2 diabetes, dyslipidemia, or hypertension)

- Morbid obese patients (BMI>35)

Exclusion Criteria:

- Prior bariatric surgery

- Malignancy (any type)

- End stage renal disease

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Procedure:
Bariatric surgery
Laparoscopic or Robot R-Y gastric bypass

Locations

Country Name City State
Korea, Republic of Hanyang University Hospital Seoul

Sponsors (1)

Lead Sponsor Collaborator
Hanyang University

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in Glomerular filtration rate before, 6, 12month after surgery No
Secondary Change in excessive body weight before, 6, 12month after surgery No
Secondary Systolic function (EF) measured by echocardogram Before, 6 and 12month after surgery No
Secondary Diastolic function (E,A,DT,IVRT,E/e') measured by echocardogram Before, 6 and 12month after surgery No
Secondary Change of daytime blood pressure (systolic blood pressure, diastolic blood pressure, mean blood pressure) measured by 24 hours ambulatory blood pressure monitoring Before, 6, and 12month after surgery No
Secondary Change of night time blood pressure (systolic blood pressure, diastolic blood pressure, mean blood pressure) measured by 24 hours ambulatory blood pressure monitoring Before, 6, and 12month after surgery No
Secondary Change of 24 hours blood pressure (systolic blood pressure, diastolic blood pressure, mean blood pressure) measured by 24 hours ambulatory blood pressure monitoring Before, 6, and 12month after surgery No
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