Kerecis Real World Registry

Status Not yet recruiting

Clinical Trial Summary

Multi-center, observational (i.e., non-interventional), open-label, real-world Registry on the Use of Kerecis Devices

Clinical Trial Description

This observational (i.e., non-interventional), post-market, real-world, Registry was designed to collect, analyze, and identify relevant safety and performance outcomes for "all comers" using Kerecis devices in routine medical practice within a wide variety of United States (US) medical practice settings. These clinical data will be used at Kerecis for many purposes, which include, but are not limited to, device safety and performance evaluation as part of routine patient care and post-market clinical follow-up data commitments to regulatory authorities around the world. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06384183
Study type	Observational [Patient Registry]
Source	Kerecis Ltd.
Contact	Anne Swearingen, DBA
Phone	703 287 8752
Email	aswearingen@kerecis.com
Status	Not yet recruiting
Phase
Start date	July 2024
Completion date	June 2027

View Details

See also
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