Geko™ Cross Therapy Registry

Status Active, not recruiting

Clinical Trial Summary

The geko™ Cross Therapy REGISTRY - Wound is a prospective, observational, anonymised data collection Registry with no experimental treatment that will fulfil an unmet need for an observational Registry to provide long-term clinical data to demonstrate patient benefit and regulatory compliance.

Clinical Trial Description

The geko™ Cross Therapy REGISTRY - Wound represents a long-term project to integrate prospectively and systematically collected clinical data on all geko™ W wound devices (or W device variants) used in SC pathways for wound management allowing for the monitoring of patient outcomes during a follow-up period of up to four follow-up visits. The clinical database collected for the geko™ CTR - Wound will form part of the overall post-market clinical follow-up strategy for the device and post market surveillance to support device safety and performance. There will be up to 50 contributing centres globally. Participants are asked at the time of signing up for the geko™ Cross Therapy REGISTRY - Wound (at the recruitment / baseline visit) to attend as many follow up visits as possible (up to a maximum of 4). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05007301
Study type	Observational [Patient Registry]
Source	Firstkind Ltd
Contact
Status	Active, not recruiting
Phase
Start date	April 4, 2022
Completion date	March 2028

View Details

See also
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Geko™ Cross Therapy Registry - Wound — CTR-Wound

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms