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Study identifier: NCT07116343 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Intrapleural Ropivacaine Infusion in Cardiac Surgery

Condition: Cardiac Surgery · Coronary Artery Disease · Valvular Diseases  ·  Sponsor: Saint Petersburg State University, Russia

PhasePhase 4
Planned participants116
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

For many patients, a primary source of postoperative pain following cardiac surgery is the presence of pleural drains, which the surgeon places at the end of the operation and maintains for 1 to 3 days. One promising method of pain management after cardiac surgery is interpleural analgesia, particularly when traditional analgesic methods, such as systemic opioids or epidural anesthesia, may be limited due to the risk of complications. Interpleural analgesia involves the introduction of local anesthetics directly into the pleural cavity through drainage tubes placed after cardiac surgery. This method targets pain receptors in the chest area, providing effective analgesia without significant systemic effects. Several clinical studies have confirmed the safety and efficacy of intrapleural administration of anesthetics after thoracic surgery. The aim of this randomised double-blind placebo controlled study is to test the hypothesis that, in patients after cardiac surgery, the quality of recovery from anesthesia with intrapleural use of ropivacaine is superior to that with a placebo.

This description comes directly from the study's public registry record.

Talk to the study team

Sergey M Efremov, MD, PhD  ·  79137946090  ·  efremovsergm@gmail.com

Always discuss trial participation with your own doctor first.

Locations (2)

Saint-Petersburg university hospitalSaint Petersburg, RussiaRecruiting
Primorskiy general hospital #1Vladivostok, RussiaRecruiting

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Source record: clinicaltrials.gov/study/NCT07116343