Literature DB >> 8063043

Randomized double-blind placebo-controlled trial to evaluate the effect of the ACTH4-9 analogue ORG 2766 in IDDM patients with neuropathy.

B Bravenboer1, P H Hendrikse, P L Oey, A C van Huffelen, C Groenhout, W H Gispen, D W Erkelens.   

Abstract

In this study we report a randomized double-blind, placebo-controlled trial to evaluate the effect of ORG 2766 in IDDM patients with peripheral neuropathy. Sixty-two patients were selected based on the following criteria: abnormal vibration perception threshold above the 95th-percentile adjusted for age and/or abnormal warm temperature threshold, both measured in the right hand. The patients were randomized into two treatment groups after baseline studies: Group 1 was treated with placebo and Group 2 was treated with 3 mg of the ACTH4-9 analogue ORG 2766 every 24 h. The total study period was 1 year. After 1 year of treatment there was a significant improvement in vibration threshold in Group 1 compared to Group 2. No other parameters improved in the study period. The number of patients selected may have been too small to detect a more important treatment effect. We conclude from this study that ORG 2766 can improve vibration threshold, indicating large myelinated fibre function, but does not affect any of the other neurophysiological function tests.

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Year:  1994        PMID: 8063043     DOI: 10.1007/bf00408479

Source DB:  PubMed          Journal:  Diabetologia        ISSN: 0012-186X            Impact factor:   10.122


  38 in total

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3.  An improved automated method for the measurement of thermal thresholds. 1. Normal subjects.

Authors:  G A Jamal; S Hansen; A I Weir; J P Ballantyne
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-04       Impact factor: 10.154

Review 4.  Diabetic peripheral neuropathies.

Authors:  Y Harati
Journal:  Ann Intern Med       Date:  1987-10       Impact factor: 25.391

5.  Prevention of cisplatin neurotoxicity with an ACTH(4-9) analogue in patients with ovarian cancer.

Authors:  R G van der Hoop; C J Vecht; M E van der Burg; A Elderson; W Boogerd; J J Heimans; E P Vries; J C van Houwelingen; F G Jennekens; W H Gispen
Journal:  N Engl J Med       Date:  1990-01-11       Impact factor: 91.245

6.  Polyol pathway activity and myo-inositol metabolism. A suggested relationship in the pathogenesis of diabetic neuropathy.

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7.  Conduction velocity along human muscle fibers in situ.

Authors:  W Troni; R Cantello; I Rainero
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8.  Sodium- and energy-dependent uptake of myo-inositol by rabbit peripheral nerve. Competitive inhibition by glucose and lack of an insulin effect.

Authors:  D A Greene; S A Lattimer
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9.  Aldose reductase inhibition in diabetic neuropathy: clinical and neurophysiological studies of one year's treatment with sorbinil.

Authors:  J P O'Hare; M H Morgan; P Alden; S Chissel; I A O'Brien; R J Corrall
Journal:  Diabet Med       Date:  1988-09       Impact factor: 4.359

10.  Ganglioside treatment of genetic and alloxan-induced diabetic neuropathy.

Authors:  A Gorio; F Aporti; F Di Gregorio; A Schiavinato; R Siliprandi; M Vitadello
Journal:  Adv Exp Med Biol       Date:  1984       Impact factor: 2.622

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  2 in total

1.  Treatment of diabetic polyneuropathy with the neurotrophic peptide ORG 2766.

Authors:  G D Valk; A C Kappelle; A M Tjon-A-Tsien; B Bravenboer; K Bakker; R P Michels; C M Groenhout; F W Bertelsmann
Journal:  J Neurol       Date:  1996-03       Impact factor: 4.849

Review 2.  Is Nerve Electrophysiology a Robust Primary Endpoint in Clinical Trials of Treatments for Diabetic Peripheral Neuropathy?

Authors:  Dalal Y Al-Bazz; Andrew J Nelson; Jamie Burgess; Ioannis N Petropoulos; Jael Nizza; Anne Marshall; Emily Brown; Daniel J Cuthbertson; Andrew G Marshall; Rayaz A Malik; Uazman Alam
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  2 in total

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