At a glance
ClinicalIndex Comparison RecordN/ACompleted· 20 enrolled
Drug / intervention
Sequential Compression Devicedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Pilot Study to Establish Use of Lower Extremity Sleeve and Sequential Compression Pump Device in Patients With Upper Extremity Weakness Post-Stroke
In Brief
A clinical study evaluating Sequential Compression Device for Upper Extremity Weakness and Stroke. Completed, enrolled 20 participants across 1 site.
Detailed Summary
The primary purpose of this study is to establish that application of a Sequential Compression Device (SCD) and lower extremity (LE) sleeve applied to a hemi-paretic upper extremity is safe.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsUpper Extremity Weakness, Stroke
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
2023202420252026
First PostedSep 2022
Enrollment StartSep 2022
Primary CompletionNov 2023
TodayJul 2026
First PostedSep 10, 2022
Enrollment StartSep 27, 2022
Primary CompletionNov 14, 2023
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 3.8 years ago
Interventions
Sequential Compression Devicedevice
Calf size lower extremity sequential compression device sleeve will be placed on the weak upper extremity blow the cubital fossa and may include the hand if necessary. The device will inflate and deflate.