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| ID | Type | Description | Link |
|---|---|---|---|
| IRB Protocol #: 11074 | Other Identifier | Stanford University |
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| Name | Class |
|---|---|
| 3M | INDUSTRY |
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The purpose of this study is to evaluate the feasibility and usability of a new portable and compact wound dressing device for the treatment of small chronic skin wounds.
This is an open label study
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| SNaP application | Experimental | This is an "open label" pilot study of SNaP Advanced Wound Care System |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| SNaP Advanced Wound Care System | Device | Application of negative pressure device daily per instructions |
|
| Measure | Description | Time Frame |
|---|---|---|
| Ease of Use for Patients | Participants were given instructions to use the SNaP device home. Participants completed a questionnaire reporting whether the device was easy to use, worthwhile to use, and whether they would use the device again. Numbers responding positively to each question are presented. | Baseline up to 31 days |
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Inclusion Criteria:- Venous stasis ulcer or other chronic wound on the lower extremity that is >1.5cm and <10cm at widest point
Exclusion Criteria:- Active wound infection.
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| Name | Affiliation | Role |
|---|---|---|
| Dr. Anne Lynn S. Chang | Stanford University | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Stanford University School of Medicine | Stanford | California | 94305 | United States |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 25901554 | Background | Fong KD, Hu D, Eichstadt SL, Gorell E, Munoz CA, Lorenz HP, Chang AL. Initial clinical experience using a novel ultraportable negative pressure wound therapy device. Wounds. 2010 Sep;22(9):230-6. |
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No sharing
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| ID | Title | Description |
|---|---|---|
| FG000 | SNaP Application | This is an "open label" pilot study of SMart Negative Pressure (SNaP) Advanced Wound Care System SNaP Advanced Wound Care System: Application of negative pressure device daily per instructions SNaP: Daily use SNaP: Daily application per protocol |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
12
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| ID | Title | Description |
|---|---|---|
| BG000 | Open Label Single Arm Study | Eligible participants |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Categorical | Count of Participants |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | ||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | Ease of Use for Patients | Participants were given instructions to use the SNaP device home. Participants completed a questionnaire reporting whether the device was easy to use, worthwhile to use, and whether they would use the device again. Numbers responding positively to each question are presented. | All participants | Posted | Number | participants | Baseline up to 31 days |
|
|
1 month
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Eligible Participants | This is an "open label" pilot study of SNaP Advanced Wound Care System SNaP Advanced Wound Care System: Application of negative pressure device daily per instructions SNaP: Daily use SNaP: Daily application per protocol |
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| Term | Organ System | Source Vocabulary | Assessment Type | Notes | Statistical Information |
|---|---|---|---|---|---|
| wound pain | Skin and subcutaneous tissue disorders | CTCAE (Unspecified) | Systematic Assessment |
Open label design without comparator arm
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Anne Chang, MD | Stanford University | (650) 721 7151 | alschang@stanford.edu |
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| ID | Term |
|---|---|
| D014456 | Ulcer |
| D014947 | Wounds and Injuries |
| ID | Term |
|---|---|
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| SNaP | Other | Daily use |
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| SNaP | Other | Daily application per protocol |
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| Participants |
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| Age, Continuous | Median | Full Range | years |
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| Sex: Female, Male | Count of Participants | Participants |
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| Region of Enrollment | Number | participants |
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| 0 |
| 12 |
| 4 |
| 12 |
| ipsilateral knee pain | Musculoskeletal and connective tissue disorders | CTCAE (Unspecified) | Systematic Assessment | 11 patients that used device lower extremity were at risk |
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