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NEUROLOGY 1998;51:1057-1062
© 1998 American Academy of Neurology

A multicenter trial of ropinirole as adjunct treatment for Parkinson's disease

A. Lieberman, MD, C. W. Olanow, MD, FRCPC, K. Sethi, MD, P. Swanson, MD, C. H. Waters, MD, S. Fahn, MD, H. Hurtig, MD, M. Yahr, MD and the Ropinirole Study Group*

From the Barrow Neurological Institute (Dr. Lieberman), Phoenix, AZ; the Mount Sinai School of Medicine (Drs. Olanow and Yahr), New York, NY; the Medical College of Georgia (Dr. Sethi), Augusta, GA; the University of Washington School of Medicine (Dr. Swanson), Seattle, WA; the University of Southern California (Dr. Waters), Los Angeles, CA; the Neurological Institute of New York (Dr. Fahn), Columbia University, New York, NY; and the Graduate Hospital (Dr. Hurtig), Philadelphia, PA.

Address correspondence and reprint requests to Dr. Abraham Lieberman, Barrow Neurological Institute, 222 W. Thomas Road, Suite 401, Phoenix, AZ 85013-4496.

Objective: To evaluate the nonergot dopamine agonist ropinirole as an adjunct to L-dopa in a randomized, double-blind trial in PD patients with motor fluctuations.

Background: L-dopa in the treatment of PD is associated with motor fluctuations, dyskinesia, and other adverse effects. The use of dopamine agonists in the treatment of PD delays recourse to L-dopa and thus delays the possibility of adverse effect onset.

Methods: Ropinirole (n = 95) or placebo (n = 54) was added to L-dopa, and L-dopa was then reduced in a planned manner during the 6-month trial.

Results: A significantly greater number of ropinirole patients were able to achieve a 20% or greater reduction in both L-dopa dose and in percent time spent "off" compared with placebo (35.0% versus 13.0%; p = 0.003). The mean daily L-dopa dose was reduced significantly with ropinirole treatment (242 mg versus 51 mg; p < 0.001) was the percent awake time spent "off" (11.7% versus 5.1%; p = 0.039). There was no difference in the percent of patients who withdraw because of adverse effects (15.8% on ropinirole versus 16.7% on placebo).

Conclusions: Ropinirole permits a reduction in L-dopa dose with enhanced clinical benefit for PD patients with motor fluctuations.


*See the Appendix on page 1061 for a list of investigators and institutions of the Ropinirole Study Group.

Supported by SmithKline Beechman (SB) Pharmaceuticals.

Presented in part at the 48th annual meeting of the American Academy of Neurology; San Francisco, CA; March 1996.




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