Post-Market Clinical Follow-up Study to Assess the Safety, Performance, and Clinical Benefit of the CE-marked Drainova® ArgentiC Catheter

Status: Recruiting
Location: See all (12) locations...
Intervention Type: Device
Study Type: Observational
SUMMARY

The goal of this observational study is to learn about the performance of the drainova® ArgentiC Catheter in clinical routine, which is used to treat fluid accumulations in hollow body structures. The device is already on the market and participants receive the catheter as part of their regular treatment. The main questions of this study are: * Does the device function as intended? * Are there any other safety risks that have not been identified? * Does it lower the symptoms of the patients as intended? Doctors and patients will answer questions regarding the improvement of the patients´ symptoms and if there were any problems with the catheter.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients ≥ 18 years old

• Patients being able to give informed consent

Locations
Other Locations
Germany
Universitätsklinikum Augsburg
RECRUITING
Augsburg
Charité Universitätsmedizin Berlin
RECRUITING
Berlin
Klinikum Chemnitz gGmbH
RECRUITING
Chemnitz
Klinikum Chemnitz gGmbH MVZ Flemmingstraße
RECRUITING
Chemnitz
Universitätsklinikum Freiburg
RECRUITING
Freiburg Im Breisgau
Universitätsklinikum Freiburg
RECRUITING
Freiburg Im Breisgau
Medizinische Hochschule Hannover
RECRUITING
Hanover
Universitätsklinikum Heidelberg
RECRUITING
Heidelberg
Lungenklinik Hemer
RECRUITING
Hemer
Clemenshospital
RECRUITING
Münster
Krankenhaus Barmherzige Brüder
RECRUITING
Regensburg
Universitätsklinikum Regensburg
RECRUITING
Regensburg
Contact Information
Primary
Natasa Mitrovic, MSc
natasa.mitrovic@lsmedcap.com
+49 7471 9849 9529
Backup
Heidrun Steinle, Dr
heidrun.steinle@lsmedcap.com
+49 7471 9848 0175
Time Frame
Start Date: 2024-06-26
Estimated Completion Date: 2026-08
Participants
Target number of participants: 162
Related Therapeutic Areas
Sponsors
Collaborators: LS medcap GmbH
Leads: ewimed GmbH

This content was sourced from clinicaltrials.gov