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.
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
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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
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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