Skip to content

Intensified Multifactorial Intervention in Patients With Type 2 Diabetes and Microalbuminuria

Intensified Multifactorial Intervention in Patients With Type 2 Diabetes and Microalbuminuria

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00320008
Acronym
Steno-2
Enrollment
160
Registered
2006-04-27
Start date
1992-01-31
Completion date
2025-12-31
Last updated
2019-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Type 2 Diabetes

Brief summary

The purpose of this study is to determine whether intensified multifactorial intervention comprising both behaviour modification and polypharmacy can reduce the risk for late diabetic complications compared to standard treatment in patients with type 2 diabetes and microalbuminuria.

Detailed description

The overall description of the Steno-2 Study is stated in four protocols approved by the regulatory authorities in Denmark. The protocol identification numbers are KA 92071gm (4 years intervention ), KA-99035g (8 years intervention ), KA-99035-GS (13 years follow-up since intervention start) and H-KA-99035-GS (21 year follow-up since intervention start). The aim of the study was to determine whether intensified multifactorial intervention comprising both behaviour modification and polypharmacy can reduce the risk for late diabetic complications compared to standard treatment in patients with type 2 diabetes and microalbuminuria. The primary end point after four years of intervention was to progression to diabetic nephropathy with other microvascular complications as secondary end points. The primary end point after eight years of intervention was a composite CVD endpoint with microvascular complications as secondary end points. The interventional part of the study was ended in December 2001 after a total of eight years of intervention. From that time on, all patients were followed in a post-trial study. Also, during post-trial period all patients in both original treatment arms received similar treatment resembling the treatment given in the original intensive arm of the study. The aim of the post-trial follow-up was to investigate the effect of intensified multifactorial intervention on i) mortality and ii) years of life gained, respectively, with such an interventional approach. Endpoints in the two parts of the post-trial follow-up: Part one at 13 years since start of intervention: Primary endpoint: Total mortality. Secondary endpoints: Cardiovascular endpoints as defined previously; Microvascular disease. Part two at 21 years since start of intervention: Primary endpoint: Difference in median time to 50% mortality in each of the two original treatment groups Secondary endpoints: Cardiovascular endpoints as defined previously; Recurrent cardiovascular events; Microvascular disease.

Interventions

BEHAVIORALDiet
BEHAVIORALExercise
BEHAVIORALStop smoking
DRUGGlucose lowering therapy
DRUGBlood pressure lowering therapy
DRUGLipid lowering therapy

Sponsors

Peter Gæde
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Type 2 diabetes * Microalbuminuria

Exclusion criteria

* Stimulated serum C-peptide concentration less than 600 pmol/L * Pancreatic insufficiency or diabetes secondary to pancreatitis * Alcohol abuse * Non-diabetic kidney disease * Life-threatening disease with death probable within 4 years of study start

Design outcomes

Primary

MeasureTime frame
Diabetic nephropathyFour years
Combined cardiovascular endpointEight years
Total mortality13 years
Years of life years gained21 years

Secondary

MeasureTime frame
Coronary interventions22 years
Amputations22 years
Vascular surgery22 years
All cause mortality22 years
Diabetic nephropathy22 years
Diabetic neuropathy22 years
Diabetic retinopathy22 years
Cardiovascular disease mortality22 years
Stroke22 years
Myocardial infarction22 years

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 6, 2026