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Parallel-Group Study to Assess the Effect of Rasagiline on Cognition in Patients With Parkinson's Disease
NCT01723228 · View on ClinicalTrials.gov ↗
Study Summary
This is a 24-week, multicenter, randomized, double-blind, placebo-controlled, add-on, parallel-group study to evaluate the effect of rasagiline on cognitive function in adults with mild cognitive impairment (MCI) in Parkinson's disease (PD-MCI).
Conditions Studied
Interventions
- DRUG Placebo
- DRUG Rasagiline
Study Locations (20)
Florida
- Teva Investigational Site 015 — Boca Raton
- Teva Investigational Site 021 — Jacksonville
- Teva Investigational Site 033 — Ormond Beach
- Teva Investigational Site 020 — Port Charlotte
- Teva Investigational Site 017 — St. Petersburg
California
- Teva Investigational Site 004 — Irvine
- Teva Investigational Site 016 — La Jolla
- Teva Investigational Site 042 — Long Beach
- Teva Investigational Site 041 — San Bernardino
Connecticut
- Teva Investigational Site 035 — Danbury
- Teva Investigational Site 034 — Manchester
- Teva Investigational Site 037 — New London
Colorado
- Teva Investigational Site 048 — Denver
- Teva Investigational Site 038 — Englewood
Illinois
- Teva Investigational Site 003 — Chicago
- Teva Investigational Site 006 — Chicago
Alabama
- Teva Investigational Site 036 — Birmingham
Arizona
- Teva Investigational Site 047 — Sun City
District of Columbia
- Teva Investigational Site 026 — Washington D.C.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 170 participants |
| Start Date | 2012-11 |
| Est. Completion | 2015-01 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01723228
The ClinicalTrials.gov registry entry for NCT01723228 describes a study currently listed as completed. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 170 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Teva Branded Pharmaceutical Products R&D, which has 103 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Parkinson's Disease appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT01723228 reports 20 study locations spanning 9 distinct geographic areas — top geographies include Florida, California, Connecticut. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT01723228 about?
NCT01723228 is a clinical study titled "Parallel-Group Study to Assess the Effect of Rasagiline on Cognition in Patients With Parkinson's Disease". This is a 24-week, multicenter, randomized, double-blind, placebo-controlled, add-on, parallel-group study to evaluate the effect of rasagiline on cognitive function in adults with mild cognitive impairment (MCI) in Parkinson's disease (PD-MCI).
What is the current status of trial NCT01723228?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 170 participants. The study started on 2012-11. Estimated completion is 2015-01.
What conditions does trial NCT01723228 study?
This clinical trial studies the following conditions: Parkinson's Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01723228?
The interventions under investigation include: Placebo (DRUG), Rasagiline (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01723228?
This trial is sponsored by Teva Branded Pharmaceutical Products R&D, which has 103 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01723228 being conducted?
This trial has 20 study locations across Alabama, Arizona, California, Colorado, Connecticut. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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