respond registry
A Prospective, MultiCenter, large, REAL-WORLD EFFECTIVENESS STUDY FOR PURAPLY® AM
The Real-World Effectiveness Study of PuraPly® AM on Wounds (RESPOND) was the first prospective, large (N=307), multicenter (28 sites) cohort study to assess the effectiveness of PuraPly® AM in various difficult-to-heal wounds.
In a primarily elderly population with large, deep, refractory wounds of long durations, use of PuraPly® AM as an antimicrobial barrier resulted in 86% of all wounds demonstrated improvement in the wound bed condition. Additionally, 41.5% of wounds achieved complete closure at 12 weeks.1
Study Background
PURAPLY® AM supported healing
in Challenging wounds
The largest real-world effectiveness study demonstrating that
PuraPly® AM supports healing and granulation tissue formation1
the study
THE RESULTS
N=307
28 Sites
Prospective, multicenter
cohort study1
Large
Difficult-to-Heal
Wounds
12.9 cm2 mean wound area1
of wounds demonstrated improvement
in wound bed conditions1
of wounds achieved > 75% reduction
in volume1
REDUCTION IN WOUND AREA, DEPTH, AND VOLUME
of wounds achieved
> 60% reduction in area1,*
at baseline
of wounds achieved
> 60% reduction in depth1,*
at baseline
of wounds achieved
> 60% reduction in volume1,*
at baseline
RATES OF WOUND CLOSURE
of wounds achieved complete closure at 12 weeks1
Frequency of wound closure;
all wounds (N=307)
Median time to closure
for all wounds1
Median time to wound closure
by wound type
SUPPORTING HEALING
IN STALLED WOUNDS
See how PuraPly® AM supported healing in chronic wounds that failed ~2 years of prior therapies, or contact an Organogenesis Tissue Regeneration Specialist to see how PuraPly® AM can help your patients.
Please refer to the PuraPly AM Instructions for Use and
PuraPly XT Instructions for Use for complete prescribing information.
1. Bain MA, et al. J Comp Eff Res. 2020;9(10):691-703.