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Completed

NCT Number: NCT00349310

Profile of Depressive Symptoms in Parkinsons Disease

To explore or establish the relationship between cognitive, mood and motor symptoms in PD to scores on depression rating scales in a naturalistic setting.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Boehringer Ingelheim Investigational Site, Innsbruck, Austria

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion_Criteria:

Observation criteria:

  • are able to provide written informed consent in accordance with Good Clinical Practice (GCP) and local legislation
  • have idiopathic Parkinsons disease according to the United Kingdom Parkinsons Disease Society Brain Bank Diagnostic Criteria for Parkinsons disease
  • show no impairment of cognitive function (MMSE score ?24)
  • are with or without symptoms of depression (full range)
  • are stable on anti-Parkinson/anti-depressive treatment for at least 1 month before entering the study
  • are or are not on concomitant antidepressant treatment
  • are in the on state during the observation period
  • did not previously undergo PD surgery

Treatment and study plan

Pramipexole

Drug

Primary outcomes

  1. HADS, HAMD-17, BDI-1A, FAB (cognitive), DSM-IV (mood- part A, B, C, E) and UPDRS

    Time frame: Up to 6 months

Sponsors and collaborators

Lead sponsor

Boehringer Ingelheim

Industry

Registry information

Official study title

Profile of Depressive Symptoms in Parkinson's Disease (PRODEST-PD)

Important dates

Study start
2006
Primary completion
2006
Study completion
2006
First posted
Jul 6, 2006
Registry last updated
Dec 14, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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