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NCT02148588 · ClinicalTrials.gov registry record · NA
Peripheral Sensory Input in Central Post Stroke Pain (CPSP)
A NA study, sponsored by Washington University School of Medicine.
- Completed
- Registry status
- NA
- Development phase
- 8
- Enrollment target
NCT02148588: Completed NA study, sponsored by Washington University School of Medicine.
NCT02148588 is a NA study that has completed, run by Washington University School of Medicine. The registered enrollment target is 8 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02148588, a NA study, has completed, sponsored by Washington University School of Medicine.
- COMPLETED
- Registry status
- NA
- Development phase
- 8 participants
- Enrollment target
Study 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.
Primary Outcome
Reduction in spontaneous pain intensity in the painful extremity from baseline to 30 minutes after a peripheral nerve block.Spontaneous pain intensity was measured on 0-10 numerical rating scale (NRS), where 0 represents "no pain", and 10 represents "worst pain imaginable"
Interventions
- DRUG Ultrasound-guided peripheral nerve block with 2% lidocaine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 8 participants |
| Start Date | 2014-08 |
| Est. Completion | 2017-01-25 |
| Phase | NA |
What the finished NCT02148588 record still lists
NCT02148588 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which Ultrasound-guided peripheral nerve block with 2% lidocaine is the first listed.
NCT02148588 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02148588 about?
NCT02148588 is a clinical study titled "Peripheral Sensory Input in Central Post Stroke Pain (CPSP)". 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.
What is the current status of trial NCT02148588?
This trial is currently completed. It is a NA study. The enrollment target is 8 participants. The study started on 2014-08. Estimated completion is 2017-01-25.
What interventions are being tested in trial NCT02148588?
The interventions under investigation include: Ultrasound-guided peripheral nerve block with 2% lidocaine (DRUG).
Who is sponsoring clinical trial NCT02148588?
This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02148588's enrollment target sits among peer trials
8 1976th of 2000 higher than 19 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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