Intrapleural Ropivacaine Infusion in Cardiac Surgery

Recruiting Phase 4 Interventional Study
Cardiac Surgery Coronary Artery Disease Valvular Diseases
Prior Safety Data This treatment has already been tested in at least one earlier human trial.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
116 (estimated)
Sponsor
Saint Petersburg State University, Russia · Other
Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial
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 lim…
Trial Locations
Loading…

Loading trial locations…

Eligibility Criteria
Inclusion Criteria: * Scheduled cardiac surgery using a standard median sternotomy. * Planned opening of the pleural cavities. * Age more than 18 years. * Signed informed consent to participate in the study. Exclusion Criteria: * Contraindications for ropivacaine * Redo surgery
Contacts

Sergey M Efremov, MD, PhD

79137946090

efremovsergm@gmail.com

CONTACT