Study of SANTYL® vs Hydrogel (SoloSite®) for Pressure Ulcers

Stopped early · Phase 4

Conditions studied: Pressure Ulcer

In brief

This study is designed to compare SANTYL® versus hydrogel (SoloSite®) in the treatment of pressure ulcers for participants in a long-term care facility. After meeting study criteria, participants will be randomly assigned for application of SANTYL® or SoloSite® to their pressure ulcer for up to 6 weeks. A study previously conducted showed that in the long-term care setting, the removal of dead skin (debridement) with SANTYL® resulted in more participants achieving complete debridement, more rapidly than when SoloSite® is used. The goal of the present study is to confirm the results of the earlier study, demonstrating superior debridement outcomes for pressure ulcers of patients in long-term care as compared to ulcers managed with SoloSite®.

Key facts

Study ID
NCT02718625
Run by
Smith & Nephew, Inc.
People needed
3
Starts
2016-08-01
Expected to finish
2017-03-09
Last updated by the study team
2020-03-10

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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