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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 Jul 23, 2026, 3:57 AM 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

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

  • Rotigotine Drug
  • Placebo Other

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
Jan 31, 2013
Primary completion
Dec 31, 2013
Completion
Feb 28, 2014
Last update posted
Aug 30, 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 30, 2018 · Synced Jul 23, 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 protocol, eligibility criteria, and contact information for NCT01782222 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →