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Renal Denervation in Diabetes.

Phase 4
Withdrawn
Conditions
Diabetes
Interventions
Procedure: Renal denervation
Registration Number
NCT02081989
Lead Sponsor
Monash University
Brief Summary

Renal denervation (the use of radio waves to oblate the renal artery) has been shown to be an effective treatment for high blood pressure. It is currently being tested in heart failure patients and we would now like to look it its effects on diabetes.

We therefore plan to enrol 20 participants with type II diabetes into this study. Half will undergo renal denervation in addition to their standard care and the other half will act as controls and only receive standard care. Treatment allocation will be randomly assigned.

All participants will undergo screening (including a physical exam, blood tests, ultrasounds and a muscle biopsy). All patients will have follow up tests (including physical exams and blood tests) 1, 3 and 6 months later.

Detailed Description

Not available

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • Over 18 years
  • Able and willing to provide informed consent
  • Patients with established type II diabetes mellitus (HbA1C>7%, diet or oral hypoglycaemic agents)
  • Clinical stable as demonstrated by no change in background anti-diabetic medication in the last 30 days.
  • Anticipated that patients are able to maintain a stable dose of medication for the duration of the study
Exclusion Criteria
  • Renal arterial anatomy ineligible for RDN: main renal arteries <4 mm in diameter or <20 mm in treatable length; multiple renal arteries where main renal artery is estimated to supply <75% of the kidney; haemodynamically or anatomically significant renal artery abnormality or stenosis in either renal artery which, in the investigator's opinion, would interfere with safe cannulation of the renal artery or require surgical repair or interventional dilation
  • History of prior renal artery intervention including balloon angioplasty, stenting or previous renal denervation.
  • Single functioning kidney
  • Need for insulin (interferes with euglycemic clamp testing) or GLP-I analogues
  • eGFR <30 ml/min (MDRD formula)
  • Any medical condition which, in the investigators opinion, may adversely affect the participants safety in the trial

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
DenervationRenal denervationRenal denervation
Primary Outcome Measures
NameTimeMethod
Glycemic control6 months

Change in glycemic control at 6 months.

glucose uptake into peripheral skeletal muscle6 months

To assess glucose uptake into peripheral skeletal muscle

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Alfred Hospital

🇦🇺

Melbourne, Victoria, Australia

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