COmedication Study Assessing Mono- and cOmbination Therapy With Levodopa-carbidopa inteStinal Gel

NCT03362879 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 412

Last updated 2020-01-06

Study results available
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Summary

The purpose of this study is to evaluate treatment of advanced Parkinson's Disease (PD) patients on levodopa-carbidopa intestinal gel (LCIG) monotherapy in a routine clinical setting.

Conditions

  • Parkinson's Disease (PD)

Sponsors & Collaborators

Principal Investigators

  • AbbVie Inc. · AbbVie

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-12-14
Primary Completion
2018-12-17
Completion
2018-12-17

Countries

  • Austria
  • Canada
  • Croatia
  • Czechia
  • Greece
  • Hungary
  • Ireland
  • Israel
  • Romania
  • Spain
  • Sweden

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03362879 on ClinicalTrials.gov