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NCT03584100 · ClinicalTrials.gov registry record · NA
Effect of Pneumatic Tourniquet on Arm Swelling After Lymph Node Removal
A NA study of Healthy Subject, sponsored by Stanford University.
- Completed
- Registry status
- NA
- Development phase
- 12
- Enrollment target
- 1
- Study location
NCT03584100 is a NA study of Healthy Subject that has completed, run by Stanford University. The registered enrollment target is 12 participants, below the 247-participant average among 16 other Healthy Subject trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.
The verdict
NCT03584100, a NA study of Healthy Subject, has completed, sponsored by Stanford University.
- COMPLETED
- Registry status
- NA
- Development phase
- 12 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of the proposed study is to evaluate the acute impact of swelling caused by low-pressure tourniquet use in the setting of ipsilateral prior axillary lymph node dissection and the change in swelling reduction following tourniquet use in three limb postures versus healthy volunteers.
Conditions Studied
Interventions
- DEVICE Tourniquet 8000
Study Locations (1)
California
- Stanford University School of Medicine - Palo Alto
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2018-11-07 |
| Est. Completion | 2020-06-30 |
| Phase | NA |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03584100
The ClinicalTrials.gov registry entry for NCT03584100 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 12 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 247-participant average among 16 other Healthy Subject trials with a reported enrollment target (95% lower). The listed sponsor is Stanford University, which has 1,744 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Healthy Subject appearing as the primary indexed condition, and to 1 intervention - of which Tourniquet 8000 is the first listed.
NCT03584100 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT03584100 about?
NCT03584100 is a clinical study titled "Effect of Pneumatic Tourniquet on Arm Swelling After Lymph Node Removal". The purpose of the proposed study is to evaluate the acute impact of swelling caused by low-pressure tourniquet use in the setting of ipsilateral prior axillary lymph node dissection and the change in swelling reduction following tourniquet use in three limb postures versus healthy volunteers.
What is the current status of trial NCT03584100?
This trial is currently completed. It is a NA study. The enrollment target is 12 participants. The study started on 2018-11-07. Estimated completion is 2020-06-30.
What conditions does trial NCT03584100 study?
This clinical trial studies the following conditions: Healthy Subject.
What interventions are being tested in trial NCT03584100?
The interventions under investigation include: Tourniquet 8000 (DEVICE).
Who is sponsoring clinical trial NCT03584100?
This trial is sponsored by Stanford University, which has 1,744 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT03584100 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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