Not Yet RecruitingPhase 2ACTRN12612000864820

Investigation of whether metformin can be used safely and effectively in patients with type 2 diabetes on peritoneal dialysis

A short term study of safety and glycaemic outcomes in peritoneal dialysis patients with type 2 diabetes treated with metformin


Sponsor

Tilenka Thynne

Enrollment

6 participants

Start Date

Sep 1, 2012

Study Type

Interventional

Conditions

Summary

This is a study aiming to evaluate whether metformin, an antidiabetic medication, can be used safety and effectively in patients with type 2 diabetes who are receiving peritoneal dialysis for their end stage kidney disease. The study runs over 4 weeks of active treatment, 250mg of metformin daily orally. We hypothesise that metformin can be safely used in patients with type 2 diabetes with end stage renal failure if dosed based on predicted drug clearance.


Eligibility

Sex: Both males and femalesMin Age: 18 YearssMax Age: 100 Yearss

Inclusion Criteria4

  • (1)>18 years old
  • (2)Type 2 DM
  • (3)Peritoneal Dialysis treatment of chronic kidney disease
  • (4)Patients in whom metformin would be used if they had normal renal function

Exclusion Criteria3

  • (1)Any patient in whom metofrmin would not be used in the setting of normal renal function- moderate-severe heart failure, liver failure, alcohol abuse, major psychaitric disorder, acutely unwell or otherwise medically unstable.
  • (2)Unability or unwilling to measure own blood glucose concentrations via glucometer.
  • (3)Inability to provide written informed consent.

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Interventions

Metformin 250 mg orally (half a 500mg tablet once a day) for 4 weeks of active treatment while continuing participants' existing peritoneal dialysis treatment. Peritoneal dialysis is not standardised

Metformin 250 mg orally (half a 500mg tablet once a day) for 4 weeks of active treatment while continuing participants' existing peritoneal dialysis treatment. Peritoneal dialysis is not standardised


Locations(1)

Australia

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ACTRN12612000864820


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