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Blood Pressure Control for Type 2 Diabetes

Blood Pressure Control to Reduce Renal Risk for Type 2 Diabetes Mellitus

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03477786
Acronym
BM4DM
Enrollment
1500
Registered
2018-03-26
Start date
2013-10-28
Completion date
2023-12-31
Last updated
2018-03-26

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

Conditions

Hypertension, Type 2 Diabetes Mellitus

Brief summary

The BP4DM study was initiated as a prospective randomized controlled trial to investigate the renal protection effect for tight blood pressure control for Taiwanese T2DM patients without previously diagnosed CV events. We set our primary outcome for the prevention of microalbuminuria development. The secondary outcomes include mortality, annual renal function declining rate, and development of cardiovascular events. The recruitment period for the RCT trial is from 2013 Oct to 2019 Dec. In addition, we also intend to continuously follow up all our recruited hypertensive diabetes patients for at least 10 years to observe their clinical outcomes including cardiovascular, renal, retinal outcomes and mortality.

Detailed description

The evidence from previous literature shows importance of the blood pressure control in T2DM. About 20% (16-29%) reduction in microalbuminuria development can be reached by continuously lowering blood pressure level from 154/87 mmHg to 144/82 mmHg (the UKPDS), to 134.7/74.8 mmHg (the ADVANCE study), and even to 119.3/64.4 mmHg (the ACCORD study). However, several limitations are also inherent in the above well-known studies. First, most of the recruited participants previous trials were Caucasians. Although 3293 Chinese patients were recruited in the ADVANCE study, they only accounted for 29.6% of total enrollees in that trial. The representative of Asian population is inadequate. There is also lack of domestic evidence-based guideline designated for Taiwanese T2DM patients in optimizing their blood pressure control. In addition, some characteristics in Asian T2DM population are different from what have been observed in the Caucasian T2DM patients. For example, there is BMI discrepancy between T2DM in Western and Eastern countries, more ACEi/ARB side effects (e.g., cough) observed in Asian population, and the possible difference in CKD/ESRD incidence in T2DM between different ethnic groups. Moreover, the enrollees in most well-known trials (e.g., ADVANCE and ACCORD studies) were those who suffered from at least one cardiovascular risk factor for secondary prevention. To our best knowledge, there is no study designed to evaluate effectiveness of blood pressure control for T2DM patients without previous CV events. Therefore, we initiated a prospective randomized controlled trial to investigate the renal protection effect for tight blood pressure control for Taiwanese T2DM patients without previously diagnosed CV events. We set our primary outcome for the prevention of microalbuminuria development to partly respond to the urgent need for this society in solving the huge burden caused by the high incidence and prevalence of diabetic nephropathy in Taiwan. The study includes two parts: (1) a RCT trial, (2) an observational cohort study. The recruitment period of this study is from 2013 Oct to 2019 Dec. The RCT trial will be ended in 2019 Dec. In addition, we also intend to continuously follow up all our recruited hypertensive diabetes patients for at least 10 years to observe their clinical outcomes including cardiovascular, renal, retinal outcomes and mortality (the part of the observational cohort study).

Interventions

COMBINATION_PRODUCTdrug adjustment and behavioral modification

anti-hypertension drug prescription by physician and case management by health educator

Sponsors

National Health Research Institutes, Taiwan
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
30 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

(for both RCT trial and observational cohort study): * type 2 DM with hypertension

Exclusion criteria

(for both RCT trial and observational cohort study): * ACR\>300 mg/g * prior history of severe CV events (e.g., MI, stroke, heart failure\>NYHA functional class III) * dialysis, blindness, amputation, liver cirrhosis, cancer under active treatment * pregnant women * proteinuria which is unrelated with diabetes * urinary tract stone \> 0.5 cm Stricter

Design outcomes

Primary

MeasureTime frameDescription
development of microalbuminuriaup to 10 yearsindicator of microalbuminuria: urine ACR

Secondary

MeasureTime frameDescription
mortalityup to 10 yearsall-cause mortality and CV-specific mortality
annual renal function declining rateup to 10 yearsindicator of renal function: eGFR assessed by CKD-EPI formula
development of cardiovascular eventsup to 10 yearscardiovascular events include MI, heart failure, and stroke

Countries

Taiwan

Contacts

Primary ContactChih-Cheng Hsu, DrPH
cch@nhri.org.tw886-37-246166

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026