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Prevention of Microvascular Complications in Overweight Diabetics With Surgery or Best Medicine (PROMISE)

Primary Purpose

Diabetic Kidney Disease

Status
Withdrawn
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Optimal medical treatment and surgery
Optimal medical treatment
Sponsored by
Karolinska Institutet
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Kidney Disease

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • • BMI 28 - 35 kg/m2

    • Age: 18-65 years, with T2DM
    • Estimated glomerular filtration rate (eGFR; by MDRD) between 30 and 60mL/min/1.73m2
    • Urine albumin creatinine ratio (ACR) of at least 30mg/g (microalbuminuria) in first void urine on two separate days.

Exclusion Criteria:

  • • Type 1 diabetes or a positive GAD antibody test

    • Known renal artery stenosis
    • Renal impairment for reasons unrelated to diabetes
    • Suspicion of glomerulonephritis as determined by urine sediment (>10 erythrocytes/visual field)
    • Post-renal obstruction diagnosed by ultrasound
    • Severe retinopathy (defined as high-risk proliferative diabetic retinopathy and severe visual loss according to the "Early Treatment Diabetic Retinopathy Study Severity Scale")
    • Severe DKD (CKD 4 or 5, requirement of renal replacement therapy such as dialysis or kidney transplantation)
    • Severe neuropathy (peripheral neuropathy stage 3)
    • Unacceptably high risk for general anesthesia
    • Prior extensive intra-abdominal surgery making laparoscopy complicated
    • Myocardial infarction, cerebrovascular accident, transient ischemic attack, coronary-artery bypass grafting or percutaneous transluminal coronary angioplasty within the previous 6 months
    • Cardiac failure (NYHA stage > 2)
    • Inability to stop smoking prior to inclusion
    • Pregnancy or breast feeding

Sites / Locations

  • Ersta hospital
  • St:Claraspital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Other

Arm Label

Optimal medical treatment and surgery

Optimal medical treatment

Arm Description

In the study 50 obese patients with CKD 3 andT2DM will be treated using the European Association for Study of Diabetes protocol in combination with RYGB surgery.

In the study 50 obese patients with CKD 3 andT2DM will be treated using the European Association for Study of Diabetes protocol

Outcomes

Primary Outcome Measures

Glomerular filtration rate
Renal function measurement by Iohexol clearance

Secondary Outcome Measures

Microvascular kidney damage
Microvascular kidney damage measured by Albumin/Creatinine Ratio
Glycaemic control
HbA1c and fasting plasma glucose measurements . Five day continuous glucose monitoring
peripheral nervous system function
Michigan Neuropathy Screening Instrument (MNSI) score, which includes two separate assessments: a lower extremity examination that includes inspection of the feet to identify deformities, dry skin, calluses, infection, fissure, or ulcers, and assessment of vibratory sensation and ankle reflexes
autonomic nervous system function
Autonomic neuropathy will be assessed with the RR intervals on ECG during deep breathing test
diabetic eyes complications
Using retinal photos and using the International Clinical Diabetic Retinopathy Disease Severity Scale
blood preassure
Blood pressure will be recorded with calibrated and validated electronic blood pressure equipment and appropriate sized cuff. Patients will sit in a chair in a quiet room for 5 minutes.
Lipids
Total cholesterol, low density lipoprotein, high density lipoprotein cholesterol and triglycerides will be measured

Full Information

First Posted
December 10, 2013
Last Updated
March 10, 2017
Sponsor
Karolinska Institutet
Collaborators
St. Claraspital AG
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1. Study Identification

Unique Protocol Identification Number
NCT02011178
Brief Title
Prevention of Microvascular Complications in Overweight Diabetics With Surgery or Best Medicine
Acronym
PROMISE
Official Title
Prevention of Microvascular Complications in Overweight Diabetics With Surgery or Best Medicine; a Prospectivee, Randomized, Multicenter Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2017
Overall Recruitment Status
Withdrawn
Why Stopped
No subjects have been enrolled
Study Start Date
March 2014 (undefined)
Primary Completion Date
January 2017 (Anticipated)
Study Completion Date
December 2017 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Karolinska Institutet
Collaborators
St. Claraspital AG

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background: Diabetic kidney disease (DKD) is chronic and often progresses to kidney failure,heart disease and premature death. Unfortunately, the best medical therapies available for DKD today are ultimately unable to prevent its progression, especially in obese patients.Surgical rerouting of food within the gut with a gastric bypass operation (RYGB), improves diabetes and some of its complications. The investigators propose to investigate whether RYGB in combination with best medical therapy in patients with DKD and obesity prevent further deterioration of kidney function over a 3 years follow up period. Study design: This is an international collaboration with leading centres in Sweden and Switzerland in which100 obese type 2 diabetic patients with established DKD will volunteer to be randomly assigned to receive best medical therapy with RYGB or best medical therapy without surgery. Participants will be 18-65 years with type 2 diabetes and impaired kidney function. Yearly measurements of kidney function will then be done over a period of 3 years as a primary outcome to determine whether differences in DKD can be detectable. The study will also examine and compare a) safety of the interventions, b) the health economic impact on direct healthcare costs and Quality of Life in patients as well as c) the value of a new marker of DKD in determining which patients are most likely to benefit from surgery. Overall the study will strengthen the evidence base guiding clinical decisions about the usefulness of RYGB as an add on therapy to best medical therapy in stopping progressive DKD in patients with obesity and diabetes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Kidney Disease

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Optimal medical treatment and surgery
Arm Type
Active Comparator
Arm Description
In the study 50 obese patients with CKD 3 andT2DM will be treated using the European Association for Study of Diabetes protocol in combination with RYGB surgery.
Arm Title
Optimal medical treatment
Arm Type
Other
Arm Description
In the study 50 obese patients with CKD 3 andT2DM will be treated using the European Association for Study of Diabetes protocol
Intervention Type
Procedure
Intervention Name(s)
Optimal medical treatment and surgery
Intervention Type
Procedure
Intervention Name(s)
Optimal medical treatment
Primary Outcome Measure Information:
Title
Glomerular filtration rate
Description
Renal function measurement by Iohexol clearance
Time Frame
Three years after intervention
Secondary Outcome Measure Information:
Title
Microvascular kidney damage
Description
Microvascular kidney damage measured by Albumin/Creatinine Ratio
Time Frame
3 years after intervention
Title
Glycaemic control
Description
HbA1c and fasting plasma glucose measurements . Five day continuous glucose monitoring
Time Frame
3 years after intervention
Title
peripheral nervous system function
Description
Michigan Neuropathy Screening Instrument (MNSI) score, which includes two separate assessments: a lower extremity examination that includes inspection of the feet to identify deformities, dry skin, calluses, infection, fissure, or ulcers, and assessment of vibratory sensation and ankle reflexes
Time Frame
3 years after intervention
Title
autonomic nervous system function
Description
Autonomic neuropathy will be assessed with the RR intervals on ECG during deep breathing test
Time Frame
3 years after intervention
Title
diabetic eyes complications
Description
Using retinal photos and using the International Clinical Diabetic Retinopathy Disease Severity Scale
Time Frame
3 years after intervention
Title
blood preassure
Description
Blood pressure will be recorded with calibrated and validated electronic blood pressure equipment and appropriate sized cuff. Patients will sit in a chair in a quiet room for 5 minutes.
Time Frame
3 years after intervention
Title
Lipids
Description
Total cholesterol, low density lipoprotein, high density lipoprotein cholesterol and triglycerides will be measured
Time Frame
3 years after intervention
Other Pre-specified Outcome Measures:
Title
health economics
Description
Direct healthcare resource consumption. Costs to Governments or Insurance companies plus private expenditure on health. Costs will include primary and secondary surgery, medication, laboratory tests, health provider reimbursement, private prescription charges and co-payments for medications
Time Frame
from intervention and three years forward
Title
Quality of life score
Description
Quality of life will be measured by the general health 36-item Health Survey (SF-36)
Time Frame
three years after intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: • BMI 28 - 35 kg/m2 Age: 18-65 years, with T2DM Estimated glomerular filtration rate (eGFR; by MDRD) between 30 and 60mL/min/1.73m2 Urine albumin creatinine ratio (ACR) of at least 30mg/g (microalbuminuria) in first void urine on two separate days. Exclusion Criteria: • Type 1 diabetes or a positive GAD antibody test Known renal artery stenosis Renal impairment for reasons unrelated to diabetes Suspicion of glomerulonephritis as determined by urine sediment (>10 erythrocytes/visual field) Post-renal obstruction diagnosed by ultrasound Severe retinopathy (defined as high-risk proliferative diabetic retinopathy and severe visual loss according to the "Early Treatment Diabetic Retinopathy Study Severity Scale") Severe DKD (CKD 4 or 5, requirement of renal replacement therapy such as dialysis or kidney transplantation) Severe neuropathy (peripheral neuropathy stage 3) Unacceptably high risk for general anesthesia Prior extensive intra-abdominal surgery making laparoscopy complicated Myocardial infarction, cerebrovascular accident, transient ischemic attack, coronary-artery bypass grafting or percutaneous transluminal coronary angioplasty within the previous 6 months Cardiac failure (NYHA stage > 2) Inability to stop smoking prior to inclusion Pregnancy or breast feeding
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thorell Anders, Professor
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ersta hospital
City
Stockholm
ZIP/Postal Code
116 28
Country
Sweden
Facility Name
St:Claraspital
City
Basel
ZIP/Postal Code
4058
Country
Switzerland

12. IPD Sharing Statement

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Prevention of Microvascular Complications in Overweight Diabetics With Surgery or Best Medicine

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