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Single-Use Negative Pressure Wound Therapy for Free Flap Donor Sites

Single-Use Negative Pressure Wound Therapy for Free Flap Donor Sites

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03340025
Enrollment
20
Registered
2017-11-13
Start date
2018-06-15
Completion date
2021-06-15
Last updated
2021-07-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Surgical Wound

Keywords

negative pressure wound therapy, split thickness skin graft

Brief summary

Various management options for free flap donor sites that require split thickness skin grafting exist. None has proven superior from both a patient care and a cost standpoint. Major complications occurring at these surgical sites include wound breakdown, tendon exposure, and loss of function. We seek to investigate the use of the PICO single-use negative pressure wound therapy device in these surgical sites and determine if it can yield superior results to simpler methods.

Detailed description

Many studies have addressed the use of negative pressure wound therapy (NPWT) in free flap donor sites with mixed results. It is well established that NPWT is safe and causes no harm, and no delay in healing. A previous study performed at UAB showed that NPWT in complex Head & Neck Surgery reconstruction is safe, including free flap donor sites. There have been studies that state the rate of tendon exposure is lower with NPWT in free flap donor sites, and studies that conclude there is no difference in complication rates. Current clinical practice is varied, often within a single institution. While no studies of NPWT in free flap donor sites have noted inferior results with its use, a primary reason cited for not using it is cost. Traditional NPWT using canister-based vacuum devices adds significant cost. The PICO single-use NPWT device (Smith & Nephew) is a relatively inexpensive, low-profile dressing that does not require attachment to an external canister. It is battery-powered and disposable. Empiric use on our patients undergoing split-thickness skin-grafting to free flap donor sites shows good results with minimal intra-operative effort compared to traditional bandaging. We would like to prospectively investigate the use of this low-cost NPWT device and compare it directly to the traditional post-op dressing method.

Interventions

DEVICEPICO Single Use Negative Pressure Wound Therapy System

Class II negative pressure wound therapy powered suction pump

DEVICExeroform gauze

traditional surgical dressing of xeroform gauze and padding

Sponsors

University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* \> 18 years of age * participants are able to consent for themselves * undergoing reconstructive surgery requiring split-thickness skin graft coverage of a free flap donor site (i.e., radial forearm free flap or fibula free flap)

Exclusion criteria

* \< 18 years of age * participants are unable to consent for themselves * undergoing reconstructive surgery that does not require split-thickness skin graft coverage of a free flap donor site

Design outcomes

Primary

MeasureTime frameDescription
Progression of Wound HealingBaseline through 30 daysComparison of photographs of all participants' wounds taken at post-operative Day 5, post-operative Day 14-21, and post-operative Day 30. Percentage skin graft take will be evaluated on Day 30 by blinded, independent raters. A 10x10 grid was digitally overlain on each image. The de-identified images were randomized and given to two independent raters. The raters used three criteria to assess each graft. Overall graft appearance was graded on a 1-5 scale, percent of graft take was estimated, and the presence of exposed tendon was noted for each timepoint.

Countries

United States

Participant flow

Participants by arm

ArmCount
Negative Pressure Wound Therapy
PICO Single Use Negative Pressure Wound Therapy System PICO Single Use Negative Pressure Wound Therapy System: Class II negative pressure wound therapy powered suction pump
11
Conventional Dressing
traditional surgical wound dressing of xeroform gauze and padding xeroform gauze: traditional surgical dressing of xeroform gauze and padding
9
Total20

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up22

Baseline characteristics

CharacteristicNegative Pressure Wound TherapyConventional DressingTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
5 Participants4 Participants9 Participants
Age, Categorical
Between 18 and 65 years
6 Participants5 Participants11 Participants
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
1 Participants0 Participants1 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
10 Participants9 Participants19 Participants
Region of Enrollment
United States
11 participants9 participants20 participants
Sex: Female, Male
Female
4 Participants1 Participants5 Participants
Sex: Female, Male
Male
7 Participants8 Participants15 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 110 / 9
other
Total, other adverse events
0 / 110 / 9
serious
Total, serious adverse events
0 / 110 / 9

Outcome results

Primary

Progression of Wound Healing

Comparison of photographs of all participants' wounds taken at post-operative Day 5, post-operative Day 14-21, and post-operative Day 30. Percentage skin graft take will be evaluated on Day 30 by blinded, independent raters. A 10x10 grid was digitally overlain on each image. The de-identified images were randomized and given to two independent raters. The raters used three criteria to assess each graft. Overall graft appearance was graded on a 1-5 scale, percent of graft take was estimated, and the presence of exposed tendon was noted for each timepoint.

Time frame: Baseline through 30 days

ArmMeasureValue (MEAN)
Negative Pressure Wound TherapyProgression of Wound Healing69.9 percentage of skin graft take
Conventional DressingProgression of Wound Healing75.6 percentage of skin graft take

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026