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Recruiting NCT05648266

Serratus Plane Block After Minimally Invasive Mitral Valve Repair

Conditions: Minimal Invasive Cardiac Surgery, Minimal Invasive Cardiac Surgery Mitral Valve Surgery, Serratus Anterior Plane Block

Sex: All
Ages: 18 Years – 85 Years
Phase: NA
Enrollment: 78
Sponsor: Universitätsklinikum Hamburg-Eppendorf

Location: Germany

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.

Eligibility Criteria

Inclusion Criteria:-Planned minimal invasive mitral valve repair via right anterior thoracotomyExclusion Criteria:PregenancyOpioid abuseHistoryof chronic painAllergy to local anaesthetics (in this case ropivacain)Patients who simultaneously participate in another interventional clinical trial, unless the Principal Investigators of the clinical trials give consent by mutual agreement Soft tissue infection in the area of the procedure

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05648266). StuddyBuddy aggregates publicly available trial information.