Peripheral Sensory Input in Central Post Stroke Pain (CPSP)

Completed · Not applicable

Conditions studied: Central Post Stroke Pain

In brief

Prospective, open-label study in 10 patients with Central Post Stroke Pain (CPSP). The study will evaluate the effects of peripheral nerve blockade on spontaneous pain and evoked thermal and mechanical responses in CPSP, and assesses the associated local anesthetic pharmacokinetics.

Key facts

Study ID

NCT02148588

Run by

Washington University School of Medicine

People needed

8

Starts

2014-08-01

Expected to finish

2017-01-25

Last updated by the study team

2018-05-02

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may not qualify if…

• Subjects will not be enrolled if any of the following criteria exist:
• Not giving consent to participate in the study;
• Significant psychiatric or cognitive impairment;
• Moderate to severe renal or liver failure;
• Concomitant treatment with warfarin or other anticoagulants;
• Pregnancy or lactation.

Where it is running

• Washington University School of Medicine — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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