The Management of Closed Surgical Incisions Resulting From Incisional Hernia Repair and/or Functional Panniculectomy Using the Prevena™ Customizable™ Dressing



Status:Terminated
Healthy:No
Age Range:18 - Any
Updated:12/14/2018
Start Date:May 2015
End Date:July 31, 2017

Use our guide to learn which trials are right for you!

The goal of this study is to evaluate the impact of Customizable in the management of
extensive closed surgical incisions for Subjects undergoing abdominal surgery for incisional
hernia repair and/or functional panniculectomy as compared to SOC dressing, and to
significantly reduce the SSC rate experienced by Subjects receiving Customizable vs. SOC
surgical incision dressing.


Pre-Operative Inclusion Criteria:

1. an adult 18 years old or older of either gender

2. able to provide their own informed consent

3. will undergo:

1. a functional panniculectomy with a transverse or a fleur-de-lis incision

- AND/OR -

2. an incisional hernia repair with a vertical incision at least 20 cm in length and
at least 10 cm of undermining on each side of the incision

4. BMI equal to or greater than 30

5. has maintained a stable weight for at least 3 months as determined by the Investigator
(applies to post weight loss patients only)

6. pre-operatively assessed to undergo a procedure with a CDC Wound Classification of:

1. Class I (Clean): An uninfected operative wound in which no inflammation is
encountered and the respiratory, alimentary, genital or uninfected urinary tract
is not entered

- OR -

2. Class II (Clean Contaminated): An operative wound in which the respiratory,
alimentary, genital or uninfected urinary tract are entered under controlled
conditions and without unusual contamination

7. willing and able to return for all scheduled study visits

8. if a female of child-bearing potential, must test negative on a urine pregnancy test

9. if a female of child-bearing potential, must be willing to utilize an acceptable
method of birth control (i.e. oral contraceptives, condom with spermicide, diaphragm
with spermicide, implants, IUD, injections, vaginal rings, hormonal skin patch) for
the duration of the study

Intra-Operative Inclusion Criteria:

1. continues to meet all pre-operative inclusion criteria

2. has undergone a Class I or II CDC Wound Classification procedure resulting in a closed
surgical incision able to be covered completely by Customizable dressing

Pre-Operative Exclusion Criteria:

1. has a systemic bacterial or fungal infection at the time of surgery for incisional
hernia repair and/or functional panniculectomy

2. has a remote-site skin infection at the time of surgery for incisional hernia repair
or functional panniculectomy

3. pre-operatively assessed to undergo a procedure with a CDC Wound Classification of:

1. Class III (Contaminated): Open, fresh, accidental wounds, and/or major breaks in
sterile technique or gross spillage from the gastrointestinal tract

- OR -

2. Class IV (Dirty-Infected): Old traumatic wounds with retained devitalized tissue
and those that involve existing clinical infection or perforated viscera

4. will have a transverse or fleur-de-lis incision that extends beyond the flank area and
requires moving the Subject from the supine position during surgery

5. has a known allergy or hypersensitivity to silver, or drape materials that contain
acrylic adhesives

6. has participated in a clinical study within the past 30 days

7. who, in the investigator's opinion, would have any clinically significant condition
that would impair the Subject's ability to comply with the study procedures

Post-Operative Exclusion Criteria:

1. found to meet any of the pre-operative exclusion criteria

2. determined to have a CDC Wound Classification of:

1. Class III (Contaminated): Open, fresh, accidental wounds, and/or major breaks in
sterile technique or gross spillage from the gastrointestinal tract

- OR -

2. Class IV (Dirty-Infected): Old traumatic wounds with retained devitalized tissue
and those that involve existing clinical infection or perforated viscera
We found this trial at
2
sites
200 Lothrop St
Pittsburgh, Pennsylvania 15213
Principal Investigator: Peter Rubin, MD, FACS
Phone: 412-864-2580
University of Pittsburgh Medical Center UPMC is one of the leading nonprofit health systems in...
?
mi
from
Pittsburgh, PA
Click here to add this to my saved trials
286 Westward Drive
Miami, Florida 33144
Principal Investigator: Julio L Arronte, MD
Phone: 305-846-7903
?
mi
from
Miami, FL
Click here to add this to my saved trials