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Double-Blind Evaluation of Efficacy and Tolerability of Metformin in NIDDM

  1. Timothy L Dornan, MRCP,
  2. Simon R Heller, MSCP,
  3. Gillian M Peck, SRN and
  4. Robert B Tattersal, FRCP
  1. Nottingham University and City Hospitals Nottingham, United Kingdom
  1. Address correspondence to Dr. Timothy L. Dornan, Consultant Physician, Hope Hospital, Stott Lane, Salford M6 8HD, UK.

Abstract

Objective To test the efficacy and tolerability of metformin.

Research Design and Methods An 8-mo double-blind placebo-controlled parallel-group trial was performed at University hospital diabetic clinics on 60 patients with non-insulin-dependent diabetes mellitus (NIDDM) treated by diet alone. Metformin was administered and built up to a maximum dosage of 1 g three times daily.

Results Mean HbA1 fell from 11.7 ± 0.4 to 10.3 ± 0.4% (means ± SE) on metformin but rose from 11.8 ± 0.4 to 13.3 ± 0.4% on placebo (P <0.001). Final mean fasting blood glucose was 5.1 mM lower with metformin than placebo (P <0.001). No other biochemical variable differed significantly, and weight did not change. A favorable glycemic response was not restricted to the obese. The mean final dosage of metformin was 1.7 ± 0.1 g and was well tolerated.

Conclusions Metformin achieved a 23% lower mean HbA1 than placebo without weight gain or significant unwanted effects.

  • Received November 9, 1989.
  • Accepted November 13, 1989.
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