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NCT03023150 · ClinicalTrials.gov registry record · NA
Ischemic Preconditioning as an Intervention to Improve Stroke Rehabilitation - Froedtert
A NA study of Stroke Rehabilitation and Ischemic Preconditioning, sponsored by Medical College of Wisconsin.
- Completed
- Registry status
- NA
- Development phase
- 20
- Enrollment target
- 1
- Study location
NCT03023150 is a NA study of Stroke Rehabilitation and Ischemic Preconditioning that has completed, run by Medical College of Wisconsin. The registered enrollment target is 20 participants, below the 58-participant average among 4 other Stroke Rehabilitation trials with a reported enrollment target (66% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03023150, a NA study of Stroke Rehabilitation and Ischemic Preconditioning, has completed, sponsored by Medical College of Wisconsin.
- COMPLETED
- Registry status
- NA
- Development phase
- 20 participants
- Enrollment target
- 1
- Study location
Study Summary
This study will be the first study to use ischemic preconditioning (IPC) as an intervention to improve stroke rehabilitation. IPC is a well studied, well tolerated intervention which has been shown to improve regional blood flow, motor neuron excitability and muscle function in multiple patient groups and in young, healthy subjects. Because IPC targets three physiological systems which are all affected by stroke, we hypothesize that repeated bouts of IPC during the first days to months following stroke (when the majority of recovery occurs) will make traditional rehabilitation strategies more effective.
Conditions Studied
Interventions
- OTHER Sham
- OTHER Ischemic Preconditioning
Study Locations (1)
Wisconsin
- Medical College of Wisconsin - Milwaukee
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 20 participants |
| Start Date | 2016-10 |
| Est. Completion | 2023-08 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03023150
The ClinicalTrials.gov registry entry for NCT03023150 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 20 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 58-participant average among 4 other Stroke Rehabilitation trials with a reported enrollment target (66% lower). The listed sponsor is Medical College of Wisconsin, which has 447 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Stroke Rehabilitation appearing as the primary indexed condition, and to 2 interventions - of which Sham is the first listed.
NCT03023150 reports 1 study location spanning 1 distinct geographic area - top geographies include Wisconsin.
Frequently Asked Questions
What is clinical trial NCT03023150 about?
NCT03023150 is a clinical study titled "Ischemic Preconditioning as an Intervention to Improve Stroke Rehabilitation - Froedtert". This study will be the first study to use ischemic preconditioning (IPC) as an intervention to improve stroke rehabilitation. IPC is a well studied, well tolerated intervention which has been shown to improve regional blood flow, motor neuron excitability and muscle function in multiple patient grou...
What is the current status of trial NCT03023150?
This trial is currently completed. It is a NA study. The enrollment target is 20 participants. The study started on 2016-10. Estimated completion is 2023-08.
What conditions does trial NCT03023150 study?
This clinical trial studies the following conditions: Stroke Rehabilitation, Ischemic Preconditioning, Physical and Rehabilitation Medicine.
What interventions are being tested in trial NCT03023150?
The interventions under investigation include: Sham (OTHER), Ischemic Preconditioning (OTHER).
Who is sponsoring clinical trial NCT03023150?
This trial is sponsored by Medical College of Wisconsin, which has 447 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03023150 being conducted?
This trial has 1 study location across Wisconsin. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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