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Clinical Trial Summary

Patients undergoing minimally invasive mitral valve reconstruction via small thoracotomy are randomized into two groups. The intervention group receives serratus anterior plane block after minimally invasive mitral-valve reconstruction, following 48h infusion with ropivacaine 2% continually. The control group receives a placebo pump without infusion. Primary endpoints are perceived pain using a numeric pain rating scale and opioid consumption during the hospital stay.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05648266
Study type Interventional
Source Universitätsklinikum Hamburg-Eppendorf
Contact Niklas Neumann, Dr.
Phone 004915222844008
Email n.neumann@uke.de
Status Recruiting
Phase N/A
Start date April 1, 2022
Completion date July 1, 2024

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