An interventional study of Oxygenesys(TM) Dissolved Oxygen Dressing in Critical Limb Ischemia, sponsored by Halyard Health. Terminated at 1 site in United States. Open to participants aged 21 Years and older. Per ClinicalTrials.gov, last updated 2015-10-12.
Sponsored by Halyard Health · Not applicable, Interventional, and Treatment
A Prospective, Randomized, Single-center Pilot Study of The OxyGenesys(TM) Dissolved Oxygen Dressing to Improve Chronic Wound Healing after REvascularization for Critical Limb Ischemia.
A Prospective, Randomized, controlled pilot study enrolling up to 50 subjects at a singe investigational site in the US. Subjects with atherosclerotic peripheral arteria disease (PAD) presenting with critical limb ischemia (CLI) and one or more non-healing lower extremity arterial insufficiency ulcers who are suitable candidates for revascularization procedures (endovascular or surgical) will be randomized 1:1 to:
An initial study phase will enroll up to 20 subjects (10 in each arm). Pending results of the initial study phase, the study may continue to enroll until up to 50 subjects (25 in each arm) have been enrolled.
All subjects will be followed clinically and receive wound evaluation at 1, 3, and 6 months.
343 studies on the registry are indexed under Chronic Limb-Threatening Ischemia; 70 are open to participants now.
This study's enrollment of 7 is below the median of 45 across 233 interventional studies indexed under Chronic Limb-Threatening Ischemia.
Browse Chronic Limb-Threatening Ischemia studies →Halyard Health is the lead sponsor of 7 studies on the registry; none are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
OxyGenesys(TM) Dissolved Oxygen Dressing
Device: Oxygenesys(TM) Dissolved Oxygen Dressing
Standard wound care using gauze dressings per institutional standard of care.
OxyGenesys(TM) Dissolved Oxygen Dressing
Rate of Wound Healing
Percentage reduction in target wound area (length x width).
Time frame: 3 months
Incidence of Complete Wound Closure
number of wounds undergoing complete reepithelialization without drainage or dressing requirements, maintained for at least 2 weeks.
Time frame: 3 months
| Milestone | All Study Participants |
|---|---|
| Started | 7 |
| Completed | 0 |
| Not completed | 7 |
| Withdrew: Lost to follow-up | 7 |
Percentage reduction in target wound area (length x width).
No measurements were reported for this outcome.
number of wounds undergoing complete reepithelialization without drainage or dressing requirements, maintained for at least 2 weeks.
No measurements were reported for this outcome.
Non-serious events are listed at a 0% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| All Study Participants | — | — | — |
| Age, Categorical(Participants) | All Study Participants |
|---|---|
| <=18 years | NA |
| Between 18 and 65 years | NA |
| >=65 years | NA |
| Sex: Female, Male(Participants) | All Study Participants |
|---|---|
| Female | NA |
| Male | NA |
This study is terminated, as verified in Nov 2014. You cannot join it, but the record below documents what was studied.
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