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Study identifier: NCT06515093 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study Assessing Complete Wound Healing by Comparing Surgenex® PelloGraft in Treating DFU and SanoGraft® in Treating VLU to SOC

Condition: Diabetic Foot Ulcer · Venous Leg Ulcer  ·  Sponsor: Surgenex

PhaseNA
Planned participants180
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to compare Pellograft to standard of care modalities in treating diabetic foot ulcers in human subjects, and to compare Sanograft to standard of care in treating venous leg ulcers. The study will demonstrate wound healing outcomes with comparators including time to wound epithelialization, decrease in wound size, and total number of study product applications towards healing outcome. This information is important to the Centers for Medicare and Medicaid Services (CMS) and other payors in determining coverage policy and reimbursement for this product category.

This description comes directly from the study's public registry record.

Talk to the study team

Pam McKeown  ·  480-404-3143  ·  pamela.mckeown@surgenex.com

Always discuss trial participation with your own doctor first.

Locations (2)

ILD ResearchVista, California, United StatesRecruiting
Tulsa Wound CenterTulsa, Oklahoma, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06515093