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OpenTrials
Completed

NCT Number: NCT02312375

Effects of Fimasartan on Insulin Secretion in Type 2 Diabetic Patients

This study was designed to evaluate the effect of ARB in improving insulin secretion in patients with type 2 diabetes. The investigators also aimed to evaluate if there are potential synergisms between ARB and DPP4 inhibitors in improving insulin secretion and urinary albumin secretion in diabetic patients.

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Key information

Age range

20 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Seoul National University Hospital

Seoul, 110-144, South Korea

About this study

Angiotensin II has been reported to insulin secretion in beta cells. Angiotensin II indirectly improves insulin secretion in beta cells via vasoconstriction and reduced islet blood flow. Chronic exposure to high glucose or high fat increases expression of AT1R (angiotensin type 1 receptor), leading to reactive oxidative stresses, inflammation, and apoptosis in beta cells, finally decreased insulin formation and secretion. Some studies showed the beneficial effect of blocking AT1R on insulin secretion and beta cell proliferation in animal models using angiotensin receptor blocker (ARB). Furthermore, 26 weeks of valsartan treatment improved insulin secretion in humans with impaired glucose regulation.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Aged 20~80 years
  • Type 2 diabetic patients diagnosed more than 6 months ago
  • HbA1c ≤8.5% at screening
  • No change of OAD within the 3 months before screening
  • SBP <140 mmHg and DBP <90 mmHg with anti-hypertensive drug at screening
  • SBP ≥140 mmHg or DBP ≥80 mmHg without anti-hypertensive drug at screening

Exclusion criteria

  • Type 1 diabetic patients or active insulin treatment at screening
  • Treatment with ARB or ACEi within 1 month prior to screening
  • Uncontrolled hypertension with SBP >170 mmHg or DBP >100 mmHg
  • Pregnancy or lactation
  • Elevated liver enzyme (AST or ALT > 3 times the UNL) or elevated serum Cr (≥1.5 mg/dL in men and 1.4 mg/dL in women)

Treatment and study plan

Fimasartan

Drug

16 weeks of fimasartan vs. amlodipine followed by 2 weeks of wash-out period, then crossover

Amlodipine

Drug

16 weeks of fimasartan vs. amlodipine followed by 2 weeks of wash-out period, then crossover

Primary outcomes

  1. Insulinogenic index

    Time frame: 16 week

Secondary outcomes

  1. HOMA β-cell function

    Time frame: 16 week

  2. Insulin resistance

    Time frame: 16 week

  3. Urinary albumin creatinine ratio, urinary protein creatinine ratio

    Time frame: 16 week

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Registry information

Official study title

Effects of Fimasartan on Insulin Secretion, and Interaction With DPP4 Inhibitors in Patients With Type 2 Diabetes

Important dates

Study start
2015
Primary completion
2016
Study completion
2017
First posted
Dec 9, 2014
Registry last updated
Apr 28, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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