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Completed Phase 4 Interventional Results available

Trial to Evaluate The Efficacy Of Rotigotine on Parkinson's Disease-Associated Motor Symptoms And Apathy

ClinicalTrials.gov ID: NCT01782222

Public ClinicalTrials.gov record NCT01782222. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 7:26 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Multinational, Double-Blind, Placebo-Controlled, 3-Arm, Phase 4 Study To Evaluate The Efficacy Of Rotigotine On Parkinson's Disease-Associated Apathy, Motor Symptoms, And Mood

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This trial is being conducted to assess the effects of Rotigotine over Placebo on improvement of Apathy and motor symptoms in subjects with early-stage and advanced stage idiopathic Parkinson´s Disease.

Study identification

NCT ID
NCT01782222
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
UCB BIOSCIENCES GmbH
Industry
Enrollment
122 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2013 (Type not available)
Primary completion
Jan 2014 (Actual)
Completion
Mar 2014 (Actual)
Last update posted
Aug 31, 2018

2013 – 2014

United States locations

U.S. sites
25
U.S. states
17
U.S. cities
24
Facility City State ZIP Site status
4320 Birmingham Alabama — —
4309 Oxnard California — —
4306 Ormond Beach Florida — —
4311 Palm Beach Gardens Florida — —
4313 Tampa Florida — —
4314 Decatur Georgia — —
4318 Chicago Illinois — —
4316 Winfield Illinois — —
4322 Des Moines Iowa — —
4304 Kansas City Kansas — —
4326 Springfield Massachusetts — —
4330 Ocean Springs Mississippi — —
4302 Las Vegas Nevada — —
4303 Commack New York — —
4317 New York New York — —
4323 New York New York — —
4319 Asheville North Carolina — —
4325 Charlotte North Carolina — —
4329 Akron Ohio — —
4312 Cincinnati Ohio — —
4324 Beaufort South Carolina — —
4332 Charleston South Carolina — —
4305 San Antonio Texas — —
4307 Salt Lake City Utah — —
4333 Virginia Beach Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01782222, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 31, 2018 · Synced Oct 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01782222 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →