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A Comparison of Bromocriptine (Parlodel®) and Levodopa-Carbidopa (Sinemet®) For Treatment of “De Novo” Parkinson's Disease Patients

Published online by Cambridge University Press:  18 September 2015

Israel Libman
Affiliation:
Jewish General Hospital, Montreal
Marek J. Gawel
Affiliation:
Sunnybrook Hospital, Toronto
Richard J. Riopelle
Affiliation:
Kingston General Hospital, Kingston
Sylvie Bouchard*
Affiliation:
Sandoz Canada Inc
*
Chef du Groupe Système Nervcux Central, Direction Scientifique, Laboratoires Sandoz France Ltée, 14, Boulevard Richelieu, BoÎte postale 313, 92508 Rueil Malmaison Cedex, France
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Abstract:

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Fifty-one patients were enrolled in a double-blind, parallel group, multicentre study conducted to assess short-term efficacy and tolerance of bromocriptine (Parlodel®) or L-DOPA/carbidopa (Sinemet®) in patients never treated with amantadine, ergot alkaloids or L-DOPA-based drugs. An attempt to use the lowest effective dose was made. The responder rate for each group was approximately 78%; the mean daily dose for responders was 22.5 mg of bromocriptine or 250 mg of L-DOPA/carbidopa. The overall clinical improvement in each group was 62% (bromocriptine) and 55% (L-DOPA/carbidopa) for neurological assessment and 36% (bromocriptine) and 31% (L-DOPA/carbidopa) for functional disability. Comparison between groups did not show any significant difference for both neurological and disability assessments. The most frequent side effect was nausea (L-DOPA, N = 3; bromocriptine, N=6).

Type
Original Articles
Copyright
Copyright © Canadian Neurological Sciences Federation 1987

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