Transdermal Use of Lisuride in Early Parkinson´s Disease: A double blind, randomized, Placebo and Pramipexole controlled study to evaluate the efficacy and safety of Lisuride TTS - TULEP 1

Recruitment & Eligibility

Status: Authorised-recruitment may be ongoing or finished

Sex: All

Target Recruitment: 350

Inclusion Criteria

• Male or female outpatients
• Age of > 30 years
• Newly diagnosed early-stage of idiopathic Parkinson’s disease for longest 1 year (diagnosis based on the UK Brain Bank Criteria)
• No previous Levodopa therapy (except challenge of diagnosis).
• Minimum UPDRS motor score of > 12 points.
• Mini Mental State Examination (MMSE) score of = 27.
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

a) Patient has non-idiopathic PD
b) Significant neurological symptoms not accounted for by Parkinson’s disease
c) Current diagnosis of epilepsy, history of seizures as an adult, history of stroke, or transitory ischemic attacks (TIA) within one year prior to the screening visit (visit VS)
d) history of pallidotomy, thalamotomy, deep brain stimulation or fetal tissue transplantation or other neurosurgery for Parkinson’s disease
e) History of or active hallucinations or delusions including drug-induced hallucina-tions, e.g. by dopaminergic therapy
f) Treatment with dopamine agonists within 28 days of the baseline visit (BL)
g) Pre-treatment with Levodopa (except for diagnostic challenge)
h) Pre-treatment during the last 3 months prior to baseline visit 2 or current treatment with MAO-A inhibitors, reserpine, budip-ine, alpha-methyldopa
i) Current treatment with CNS active therapy unless the dose has been stable for at least 28 days prior to the baseline visit (BL)
j) Current treatment with medications eliminated through the renal tubulus system or which inhibit the active renal tubulus secretion
k) History or presence of dementia
l) Presence of major depression
m) evidence or suspicion of any cardiac valvulopathy or any other cardiac disor-der which would put the patient at risk of clinically relevant arrhythmia and/or myocardial infarction, within the last 12 months
n) Clinically relevant hepatic dysfunction
o) Clinically relevant renal dysfunction
p) History of syncope and/or severe otherwise symptomatic orthostatic hypotension within the last year or a systolic blood pressure less than 105 mmHg at Screening Visit VS
q) History of significant skin hypersensitivity to adhesive or other transdermal applications, or recent unresolved contact dermatitis
r) Any medical or psychiatric condition or any other clinically significant laboratory abnormalities that, in the opinion of the investigator, would interfere with the ap-propriate conduct of the study
s) Alcohol or drug abuse in the past three years
t) Females of childbearing potential who are planning to become pregnant, who are pregnant or lactating and/or who are unwilling to use effective means of contracep-tion
u) Patient has previously participated in this trial or patient has previously been as-signed to treatment in a trial with Lisuride TTS
v) Participation in other clinical studies in the previous four weeks
w) Pregnancy or lactation
x) QTc > 470 ms at Visit 1 (Bazett correction must be used)
y) Known hypersensitivity to Pramipexole and/or Lisuride
z) Creatinine clearance estimated according to Cockroft and Gault < 30 ml/min

Study & Design

Study Type: Interventional clinical trial of medicinal product

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method

Secondary Outcome Measures

Name	Time	Method

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