Proteomic Prediction and Renin Angiotensin Aldosterone System Inhibition Prevention Of Early Diabetic nephRopathy In TYpe 2 Diabetic Patients With Normoalbuminuria (PRIORITY)

This study is currently recruiting participants. (see Contacts and Locations)
Verified March 2014 by Steno Diabetes Center
Sponsor:
Collaborators:
Mosaiques Diagnostics GmbH
University Medical Centre Groningen
University of Glasgow
Istituto di Richerche Farmacologiche Mario Negri
Univerzita Karlova v Praze
Charite University, Berlin, Germany
Geniko Nosokomeio Athinas Ippokrateio
Institut Klinické a Experimentální Mediciny Praze
Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz
Institut Universitaire de Recherche Clinique Montpellier
Klinikum St. Georg Leipzig
Universitaet Zürich
Cyril and Methodius University in Skopje
Hannover Clinical Trial Center
European Commission
Information provided by (Responsible Party):
Peter Rossing, Steno Diabetes Center
ClinicalTrials.gov Identifier:
NCT02040441
First received: December 16, 2013
Last updated: March 14, 2014
Last verified: March 2014
  Purpose

This is a prospective, multicenter, randomized, double blind, placebo-controlled and a prospective observational study.

This study will be conducted at 13 study centers in various European countries. Approximately 3500 participant between 18 to 75 years old with Type 2 diabetes mellitus and normoalbuminuria will participate in the study. The study period is 3 years (excluding the 6 week screening period). Depending on the risk score of the urinary protein pattern, participants will be stratified into an observational group or an interventional group. Either 5 (low risk pattern, observational group) or 15 (high risk pattern, interventional group) office visits of 1-3 hours duration are scheduled.

The interventional group will be allocated into one treatment group either receiving spironolactone or placebo. A placebo is a medicine without a pharmaceutical substance. The allocation to one of the two treatment groups will be done by a random distribution procedure established before the study start.

The results of the urine sample from the Screening visit has been analysed and the urine proteomic pattern is determined to be either low- or high risk pattern and will determine the further study program.

Participants with a low-risk pattern (observational group) (approximately 80%):

During the next three years, participants will attend an annual project visit, were regular diabetes care will be performed and three urine samples will be analysed for albuminuria.

Participants with a high-risk pattern (intervention group) (approximately 20%):

Participants with a high-risk pattern will be randomization to either spironolactone treatment or placebo. The treatment is one tablet for oral use to be ta en once a day for the next three years. Four times each year (every 13th week) a study visit will be conducted including examination of three urine samples for albuminuria.

This study aims to:

  1. Confirm in a prospective multicenter study of normoalbuminuric type 2 DM patients that the urinary proteome test identifies patients with a high risk for development of microalbuminuria.
  2. Demonstrate the clinical utility of the test by showing that aldosterone blockade in high-risk patients can reduce progression to microalbuminuria in comparison to placebo, on the top of standard treatment in a randomized double-blind, placebo-controlled multicenter study.

Condition Intervention Phase
Diabetic Nephropathy
Diabetic Retinopathy
Drug: Spironolactone
Drug: Placebo
Drug: Standard care
Phase 2
Phase 3

Study Type: Interventional
Study Design: Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor)
Primary Purpose: Diagnostic
Official Title: Proteomic Prediction and Renin Angiotensin Aldosterone System Inhibition Prevention Of Early Diabetic nephRopathy In TYpe 2 Diabetic Patients With Normoalbuminuria

Resource links provided by NLM:


Further study details as provided by Steno Diabetes Center:

Primary Outcome Measures:
  • Albuminuria [ Time Frame: Screening, (Low-risk: year 1, 2 and 3), (high-risk: week 13, 26, 39, 52, 65, 78, 91, 104, 117, 130, 143, 156) ] [ Designated as safety issue: Yes ]
    Development of confirmed microalbuminuria (UACR >30 mg/g) in at least two out of three first morning voids with ≥ 30% increase (geometric mean) in UACR from "run-in" period samples OR > 40 mg/g (geometric mean).


Secondary Outcome Measures:
  • Cardiovascular disease and mortality [ Time Frame: Screening, (Low-risk: year 1, 2 and 3), (high-risk: week 13, 26, 39, 52, 65, 78, 91, 104, 117, 130, 143, 156) ] [ Designated as safety issue: No ]
    Comparison of composite fatal and non-fatal cardiovascular outcome (myocardial infarction, stroke, coronary artery bypass, coronary re-vascularisation, hospitalization for heart failure and cardiovascular death), and all-cause mortality during the study.

  • Retinopathy [ Time Frame: Screening, (Low-risk: year 1, 2 and 3), (high-risk: week 13, 26, 39, 52, 65, 78, 91, 104, 117, 130, 143, 156) ] [ Designated as safety issue: No ]
    Comparison of incidence of retinopathy and frequency of laser treatment. Data collected from self-reported adverse events.

  • Change in albuminuria [ Time Frame: Screening, (Low-risk: year 1, 2 and 3), (high-risk: week 13, 26, 39, 52, 65, 78, 91, 104, 117, 130, 143, 156) ] [ Designated as safety issue: No ]
    In addition to the categorical analysis of urinary albumin excretion, an analysis will be performed with changes in geometric mean albuminuria throughout the study period in all patients by assessing the slope of albuminuria changes and absolute changes from inclusion to end of trial

  • Microalbuminuria [ Time Frame: Screening, (Low-risk: year 1, 2 and 3), (high-risk: week 13, 26, 39, 52, 65, 78, 91, 104, 117, 130, 143, 156) ] [ Designated as safety issue: No ]
    Development of microalbuminuria (UACR >30 mg/g) in at least one morn-ing void urine sample will be used as a secondary outcome instead of con-firmed microalbuminuria

  • Macroalbuminuria [ Time Frame: Screening, (Low-risk: year 1, 2 and 3), (high-risk: week 13, 26, 39, 52, 65, 78, 91, 104, 117, 130, 143, 156) ] [ Designated as safety issue: No ]
    Development of macroalbuminuria (UACR >300 mg/g) in 2 out 3 first morning void urine samples)

  • Change in CKD class [ Time Frame: Screening, (Low-risk: year 1, 2 and 3), (high-risk: week 13, 26, 39, 52, 65, 78, 91, 104, 117, 130, 143, 156) ] [ Designated as safety issue: No ]
    For patients with estimated GFR ≥ 60 at baseline, development of estimated GFR<60 ml/min/1.73m2. Estimated GFR will be measured from serum creatinine (standard-ized traceable method) on blood samples tested in local laboratories.

  • Slope of estimated GFR [ Time Frame: Screening, (Low-risk: year 1, 2 and 3), (high-risk: week 13, 26, 39, 52, 65, 78, 91, 104, 117, 130, 143, 156) ] [ Designated as safety issue: No ]
    Change in estimated GFR (slope and absolute from baseline and from 3 month post-baseline to end of study)


Estimated Enrollment: 3500
Study Start Date: November 2013
Estimated Study Completion Date: December 2017
Estimated Primary Completion Date: December 2017 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Active Comparator: Spironolactone
High-risk pattern: Spironolactone 25 mg once daily + Standard care
Drug: Spironolactone Drug: Standard care
Standard diabetes care
Placebo Comparator: Placebo
High-risk pattern: One placebo tablet once daily + Standard care
Drug: Placebo Drug: Standard care
Standard diabetes care
Observational
Low-risk pattern: Standard care
Drug: Standard care
Standard diabetes care

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  1. Written informed consent must be provided before participation. Patient information and consent form must be approved by relevant independent ethical committee. Specifically, all participating patients will be asked to give informed consent for long-term follow-up and collection of follow-up data
  2. Male or female patients ≥ 18 years and < 75 years of age at Screening visit
  3. Type 2 DM (WHO criteria)
  4. Persistent normoalbuminuria (at least 2 of 3 UACR < 30 mg/g samples from "run in"-period)
  5. Estimated GFR >45 ml/min/1.73m2 (MDRD formula) at Screening vi-sit
  6. HbA1c ≥ 6.5% (48 mmol / mol) and < 13% (119 mmol / mol) at Screening visit
  7. The patient must be willing and able to comply with the protocol for the duration of the study
  8. Female without child-bearing potential at the screening visit. Defined as one or more of following:

8.1) Female patients ≥ 50 years of age at the day of inclusion, who have been postmenopausal for at least 1 year 8.2) Female patients < 50 years of age at the day of inclusion, who have been postmenopausal for at least 1 year and serum follicle stimulating hormone levels > 40 milli International unit / mL as well as serum estrogen levels < 30 pg/ml or a negative estrogen test.

8.3) 6 weeks after surgical sterilization by bilateral tubal ligation or bilateral ovariectomy with or without hysterectomy.

OR a negative urine pregnancy test at the Screening visit AND one or more of following:

8.4) Correct use of reliable contraception methods. This includes one or more of the following: hormonal contraceptive (such as injection, transdermal patch, implant, cervical ring or oral) or an intrauterine device (IUD) OR correct use of double barrier with one of the following: barrier methods (diaphragm, cervical cap, Lea contraceptive or condom) AND in combination with a spermicide.

8.5) General sexual abstinence from the time of screening/ baseline, during the study until a minimum of 30 days after the last administration of study medication if this is already established as the patient's preferred and usual lifestyle.

8.6) Having only female sexual partners. 8.7) Sexual relationship with sterile male partners only

Exclusion Criteria:

  1. Average of systolic BP< 110 or >160 mm Hg at baseline
  2. Average of diastolic BP > 100 mm Hg at baseline
  3. Type 1 DM (WHO criteria)
  4. Current in treatment with more than one RAAS blocking agent (Angiotensin Converting Enzyme inhibitor, Angiotensin Receptor Blocker or Direct Renin Inhibitor)
  5. Current lithium treatment
  6. Known or suspected hypersensitivity to Spironolactone or to any of its excipients.
  7. Current use of potassium sparing diuretics, such as: Spironolactone, Eplerenone or Amiloride etc.
  8. Screening (week -6) plasma (or serum) potassium level >5.0 mmol/L
  9. Low plasma sodium determine by the investigator
  10. Current cancer treatment or within five years from baseline (except basal cell skin cancer or squamous cell skin cancer)
  11. Any clinically significant disorder, except for conditions associated with type 2 DM history, which in the Investigators opinion could interfere with the results of the trial
  12. Cardiac disease defined as: Heart failure (NYHA class III-IV) and/or diagnosis of unstable angina pectoris and/or myocardial ischemia, stroke, cardiac re-vascularisation or coronary artery bypass within the last 3 months
  13. Body mass index <18.5 or >40 kg/m2
  14. Diagnosis of non-Diabetic CKD current or in the past
  15. Diagnosis of liver cirrhosis with current impaired liver function within the last 3 years.
  16. Diagnosis of Addison's disease.
  17. Being lactating.
  18. Intend to become pregnant within the duration of the study or not use adequate birth control.
  19. Known or suspected abuse of alcohol or narcotics
  20. Not able to understand informed consent form
  21. Participation in any other intervention trial than PRIORITY or a related sub-study is not allowed within 30 days before inclusion or concurrent to this study
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT02040441

Contacts
Contact: Peter Rossing, Prof, MD +45 4443 7310 Pro@steno.dk
Contact: Morten Lindhardt, MD +45 3075 2019 mkfl@steno.dk

Locations
Denmark
Steno Diabets Center Recruiting
Gentofte, Denmark, 2820
Contact: Morten Lindhardt, MD    +45 30752019    mkfl@steno.dk   
Contact: Peter Rossing, Prof. MD    +45 4443 7310    pro@steno.dk   
Sub-Investigator: Morten Lindhardt, MD         
Principal Investigator: Peter Rossing, Prof. MD         
Italy
Instituto de Ricerche Farmacologiche Mario Negri Recruiting
Bergamo, Italy, 24020
Contact: Matias Trillini, MD       matias.trillini@marionegri.it   
Sub-Investigator: Matias Trillini, MD         
Principal Investigator: Piero Luigi Ruggenenti, MD         
Spain
Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz Active, not recruiting
Madrid, Spain, 28040
United Kingdom
University of Glasgow Recruiting
Glasgow, United Kingdom, G12 8TA
Contact: Christian Delles, DM       Christian.Delles@glasgow.ac.uk   
Principal Investigator: Christian Delles, MD         
Sub-Investigator: Gemma Currie, MD         
Sponsors and Collaborators
Peter Rossing
Mosaiques Diagnostics GmbH
University Medical Centre Groningen
University of Glasgow
Istituto di Richerche Farmacologiche Mario Negri
Univerzita Karlova v Praze
Charite University, Berlin, Germany
Geniko Nosokomeio Athinas Ippokrateio
Institut Klinické a Experimentální Mediciny Praze
Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz
Institut Universitaire de Recherche Clinique Montpellier
Klinikum St. Georg Leipzig
Universitaet Zürich
Cyril and Methodius University in Skopje
Hannover Clinical Trial Center
European Commission
Investigators
Study Chair: Peter Rossing, Prof. MD Steno Diabetes Center
Principal Investigator: Matias Trillini, MD Istituto de Ricerche Farmacologiche Mario Negri
Principal Investigator: Alberto Ortiz, MD Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz
Principal Investigator: Angel Argiles, MD Institut Universitaire de Recherche Clinique, RD Nephrologie SAS
Principal Investigator: Christian Delles, MD University of Glasgow
Principal Investigator: Gerjan Navis, MD University Medical Centre Groningen
Principal Investigator: Ivan Rychlik, MD Univerzita Karlova v Praze
Principal Investigator: Joachim Beige, MD Klinikum St. Georg gGmbH
Principal Investigator: Marina Noutsou, MD Geniko Nosikomeico Athinas Ippokrateio, Hospital Diabetes Center
Principal Investigator: Petr Boucek, MD Institut Klinické a Experimentální Mediciny
  More Information

Additional Information:
No publications provided

Responsible Party: Peter Rossing, Professor, Head of Research, Cheif Physician, MD, DMSc, Steno Diabetes Center
ClinicalTrials.gov Identifier: NCT02040441     History of Changes
Other Study ID Numbers: 2012-000452-34, 2012-000452-34
Study First Received: December 16, 2013
Last Updated: March 14, 2014
Health Authority: Denmark: Danish Health and Medicines Authority
Denmark: The Regional Committee on Biomedical Research Ethics

Keywords provided by Steno Diabetes Center:
Proteomics
Diabetes
Chronic kidney disease
Diabetic nephropathy
Diabetic retinopathy
Mineralocorticoid receptor antagonists
Spironolactone
Microalbuminuria

Additional relevant MeSH terms:
Kidney Diseases
Retinal Diseases
Diabetic Retinopathy
Diabetic Nephropathies
Urologic Diseases
Eye Diseases
Diabetic Angiopathies
Vascular Diseases
Cardiovascular Diseases
Diabetes Complications
Diabetes Mellitus
Endocrine System Diseases
Spironolactone
Mineralocorticoid Receptor Antagonists
Hormone Antagonists
Hormones, Hormone Substitutes, and Hormone Antagonists
Physiological Effects of Drugs
Pharmacologic Actions
Diuretics, Potassium Sparing
Diuretics
Natriuretic Agents
Cardiovascular Agents
Therapeutic Uses

ClinicalTrials.gov processed this record on October 19, 2014