Impaired gastric emptying may be the cause for some response fluctuati
ons in Parkinson's disease (PD), especially the ''delayed-on'' and ''n
o-on'' phenomena. Cisapride is a prokinetic drug that enhances gastric
emptying by releasing acetylcholine from the myenteric plexus. Tolera
bility and safety as well as efficacy of cisapride was studied in an o
pen-label trial on 15 fluctuating PD patients. Twelve patients had ''d
elayed-on'' and six had ''no-on'' phenomena. They filled out daily dia
ries on times of levodopa intake and of turning ''on'' and ''off'' for
1 week on levodopa alone and for an additional week of pretreatment w
ith cisapride, 30 min before early morning, early afternoon, and late
evening doses of levodopa. Cisapride significantly shortened latency t
o ''on'' from 60 +/- 20 to 45 +/- 19 min after the morning dose and fr
om 63 +/- 17 to 47 +/- 22 min after the evening doses. Patients with '
'no-on'' phenomenon had a decreased number of dose failures from 23 be
fore to nine during cisapride treatment. The drug was well tolerated,
with no important side effects. Our study supports the role of impaire
d gastric emptying in some subtypes of motor fluctuations and indicate
s that they may be improved by prokinetic drugs.