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Clinical Trial Summary

A Post-Market Clinical Follow-up (PMCF) study designed as non-interventional, observational, prospective, multicentre study in a routine clinical care setting using a marketed medical device in line with the corresponding Instruction for Use (IFU) in the intended patient population. Patients will be diagnosed and evaluated for eligibility in routine clinical care by expert centres in the indication of interest. They will be consecutively enrolled into the study provided that all inclusion and exclusion criteria are met and written consent is given to use their clinical routine data according to data privacy regulations. The study protocol does not define specific study procedures for patients enrolled. Therapies and procedures during the course of this study will be performed according to the decision of the treating physician based on current applicable medical guidelines and on local policy in clinical routine care.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05476263
Study type Observational [Patient Registry]
Source Lohmann & Rauscher
Contact Daria Trofimenko, MD
Phone +49 (0)2631- 99 6385
Email Daria.Trofimenko@de.LRmed.com
Status Not yet recruiting
Phase
Start date June 2024
Completion date September 2027

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