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OpenTrials
Completed

NCT Number: NCT00794066

Peripheral Arteriopathy Rate In Stroke

Purpose:

To assess the prevalence of peripheral arterial disease (PAD) in acute stroke patients.

Interventions:

Assessment of the ankle brachial index using the "boso-ABI-system 100" (www.boso.de).

Design:

Prospective, open, cohort study.

Study size planned:

1500.

Follow-up duration:

3 months.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Department of Neurology, University of Erlangen, Germany

Erlangen, 91054, Germany

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • All consecutive adult patients with acute ischemic or hemorrhagic stroke.

Exclusion criteria

  • Congestive heart failure.

Treatment and study plan

measuring the ankle brachial index

Procedure

Assessment of the ankle brachial index using the "boso-ABI-system 100" (www.boso.de).

Primary outcomes

  1. Functional outcome (modified Rankin Scale)

    Time frame: 3 months

Secondary outcomes

  1. Prevalence of peripheral arterial disease

    Time frame: during hospital stay

    Presence or not of PAD as assessed using ABI during hospital stay

Sponsors and collaborators

Lead sponsor

University of Erlangen-Nürnberg Medical School

Other

Registry information

Official study title

Prevalence of Peripheral Arterial Disease in Acute Ischemic and Hemorrhagic Stroke Patients

Acronym: PARIS

Important dates

Study start
2008
Primary completion
2017
Study completion
2017
First posted
Nov 19, 2008
Registry last updated
Oct 25, 2017

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

View the official ClinicalTrials.gov record (opens in a new tab)

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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