PuraPly® AM Plus the Standard of Care to Standard of Care Alone for the Management of Stage II-IV Pressure Ulcers.

O

Organogenesis

Status

Terminated

Conditions

Chronic Pressure Ulcers

Treatments

Device: PuraPly® Antimicrobial Wound Matrix
Other: SOC for Pressure Ulcers

Study type

Interventional

Funder types

Industry

Identifiers

NCT03502824
17-PRU-004-PPAM

Details and patient eligibility

About

This is a prospective, multi-center, randomized, controlled clinical study Of PuraPly® AM and standard of care (SOC) compared to SOC alone for the management of Stage II-IV pressure ulcers located in the gluteal, ischial, hip, sacral, coccygeal, and trochanteric, malleolus, or heel area.

Full description

This study seeks to demonstrate how PuraPly® AM performs against standard of care in Stage II-IV Pressure Ulcers through a prospective randomized controlled study design. Subjects may be enrolled for up to 24 weeks; if healing occurs prior to week 24, a follow up healing confirmation visit shall occur two weeks later to confirm maintenance of complete wound closure and participation may continue up to 24 weeks. Subjects that are randomized to the SOC group have the opportunity to cross over and receive PuraPly AM at week 12 if their index ulcer has not healed; they will then be followed for an additional 12 weeks for up to 24 weeks.

Enrollment

40 patients

Sex

All

Ages

18 to 99 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Subject must be at least 18 years of age.
  2. Subject has a Stage II-IV pressure ulcer located in the gluteal, ischial, hip, sacral, coccygeal, and trochanteric, malleolus, or heel area.
  3. Pressure ulcer should be present for 4 weeks duration and have a ulcer surface area > 2cm2
  4. If multiple ulcers are present, one ulcer must be identified as the index ulcer.
  5. The index ulcer is free from active infection at the time of randomization.
  6. Willingness to off-load or pressure redistribute ulcer for duration of enrollment
  7. The index ulcer has been offloaded for at least 7 days prior to randomization.
  8. The index ulcer must have been present for at least 30 days at time of study enrollment.
  9. The index ulcer is separated at least 4 cm from all other ulcers at Study Day -7 and Study Day 0 (post-debridement) and has a margin of intact skin sufficient for anchoring of the required study dressing.
  10. Subject has read and signed the IRB/IEC approved Informed Consent Form (ICF) before screening procedures are undertaken.

Exclusion criteria

  1. Presence of signs and symptoms of infection at the index ulcer site, including but not limited to cellulitis, acute osteomyelitis, excessive exudate, gangrene or deep tissue infection
  2. The index ulcer is not free of necrotic tissue and is unable to tolerate debridement
  3. Non-enteric or unexplored sinus tract
  4. Concomitant conditions that in the judgment of the investigator would make the subject inappropriate for entry to the study
  5. Subject has a known sensitivity to porcine materials
  6. Subject has a known sensitivity to polyhexamethylenebiguanide (PHMB)

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

PuraPly® AM plus Standard of Care
Active Comparator group
Treatment:
Device: PuraPly® Antimicrobial Wound Matrix
Standard of Care (SOC) for Pressure Ulcers
Active Comparator group
Treatment:
Other: SOC for Pressure Ulcers

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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