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NCT05196737 · ClinicalTrials.gov registry record · NA
DDN in Stroke--COBRE
A NA study of Stroke and Spasticity, Muscle, sponsored by Medical University of South Carolina.
- Completed
- Registry status
- NA
- Development phase
- 11
- Enrollment target
- 1
- Study location
NCT05196737: Completed NA study of Stroke and Spasticity, Muscle, sponsored by Medical University of South Carolina.
NCT05196737 is a NA study of Stroke and Spasticity, Muscle that has completed, run by Medical University of South Carolina. The registered enrollment target is 11 participants, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05196737, a NA study of Stroke and Spasticity, Muscle, has completed, sponsored by Medical University of South Carolina.
- COMPLETED
- Registry status
- NA
- Development phase
- 11 participants
- Enrollment target
- 1
- Study location
Study Summary
The study team is recruiting 20 adults with spasticity due to chronic stroke for a 7 day study over 2 weeks. In people with chronic stroke, one of the most common and disabling problems is spasticity (increased muscle tone or muscle stiffness). The purpose of this research study is to examine effects of dry needling on the nervous system (pathways between the muscle, spinal cord, and brain) in people with spasticity due to chronic stroke. Dry needling is a procedure in which a thin, stainless steel needle is inserted into the skin to produce a muscle twitch response. It is intended to release a knot in the muscle and relieve pain. The total study duration is 7 visits over 2 weeks. There will be 4 visits the first week, and 3 visits the second week. The first visit will take about 1.5 hours, during which study staff will determine the best placement of electrodes and create a cast of the participant's leg to aid them in quickly placing the electrodes on the remainder of the visits. The second and fifth visits will last about 3.5 hours, and all other visits will last about 1.5 hours. Dry needling will take place on the fifth visit only. During each visit the participant will be asked to participate in examinations of reflexes (muscle responses to non-invasive nerve stimulation) and leg function.
Primary Outcome
H-reflex amplitude (mV) reflects the excitability of its reflex pathway. Changes in the H-reflex amplitude indicate that DDN influences the spinal excitability. This will be measured in the tibialis anterior and the triceps surae.
Conditions Studied
Interventions
- BEHAVIORAL Dry Needling
Study Locations (1)
South Carolina
- Medical University of South Carolina - Charleston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 11 participants |
| Start Date | 2022-03-07 |
| Est. Completion | 2023-06-16 |
| Phase | NA |
What the finished NCT05196737 record still lists
NCT05196737 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 12,016-participant average among 454 other Stroke trials with a reported enrollment target (100% lower).
The record links to 3 conditions, with Stroke appearing as the primary indexed condition, and to 1 intervention - of which Dry Needling is the first listed.
NCT05196737 reports a single indexed study location in South Carolina.
Frequently Asked Questions
What is clinical trial NCT05196737 about?
NCT05196737 is a clinical study titled "DDN in Stroke--COBRE". The study team is recruiting 20 adults with spasticity due to chronic stroke for a 7 day study over 2 weeks. In people with chronic stroke, one of the most common and disabling problems is spasticity (increased muscle tone or muscle stiffness). The purpose of this research study is to examine effect...
What is the current status of trial NCT05196737?
This trial is currently completed. It is a NA study. The enrollment target is 11 participants. The study started on 2022-03-07. Estimated completion is 2023-06-16.
What conditions does trial NCT05196737 study?
This clinical trial studies the following conditions: Stroke, Spasticity, Muscle, CVA.
What interventions are being tested in trial NCT05196737?
The interventions under investigation include: Dry Needling (BEHAVIORAL).
Who is sponsoring clinical trial NCT05196737?
This trial is sponsored by Medical University of South Carolina, which has 755 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT05196737 being conducted?
This trial has 1 study location across South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
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Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT05196737's enrollment target sits among peer trials
11 409th of 454 higher than 41 of 454 other Stroke trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Stroke 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.
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