Peripheral Sensory Input in Central Post Stroke Pain (CPSP)

Clinical Trial Summary

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.

See also
	Status	Clinical Trial	Phase
	Completed	`NCT02277912` - Efficacy of Transcranial Magnetic Stimulation (TMS) in Central Post Stroke Pain ( CPSP)	N/A
	Not yet recruiting	`NCT06387914` - Efficacy of Pain Intervention With Deep Brain Stimulation Neuromodulation	N/A

See also

Status

Clinical Trial

Phase

Completed

NCT02277912 - Efficacy of Transcranial Magnetic Stimulation (TMS) in Central Post Stroke Pain ( CPSP)

N/A

Not yet recruiting

NCT06387914 - Efficacy of Pain Intervention With Deep Brain Stimulation Neuromodulation

N/A

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT02148588
Study type	Interventional
Source	Washington University School of Medicine
Contact
Status	Completed
Phase	N/A
Start date	August 2014
Completion date	January 25, 2017

Peripheral Sensory Input in Central Post Stroke Pain (CPSP)

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms