NCT06418100Active, not recruiting
Recto-intercostal Block for Coronary Artery Bypass Grafting
Recto-intercostal Fascial Plane Block for Postoperative Analgesia in Coronary Artery Bypass Grafting With Sternotomy: a Randomized, Double-blind, Controlled Study
Source: ClinicalTrials.gov · Last updated 19 Mar 2025
Brief summary (registry, in English)
This interventional study aims to learn about the postoperative analgesic efficacy of a new fascial plane block, recto-intercostal fascial plane block, at coronary artery bypass grafting with sternotomy. There will be two groups, one of which will be the control group, and the other will be the study group randomly receiving postoperative recto-intercostal fascial plane block. The main questions it aims to answer are the effect of this new block on postoperative opioid consumption and pain scores. Also, postoperative outcomes related to respiratory ( postoperative oxygenation and atelectasis score), hemodynamic functions ( newly developed arrhythmias), total postanesthesia care unit stay, and hospital stay will be questioned.
- Status (registry)
- Active, not recruiting
- Study type
- Interventional
- Enrollment
- 60 (estimated)
- First submitted
- 26 Feb 2024
- Start date
- 1 Mar 2024
- Primary completion date
- 1 May 2025
- Lead sponsor
- Haseki Training and Research Hospital
- Diseases
- Coronary artery disease
- NCT number
- NCT06418100
What you commit to
- Study type: Interventional
- Planned participants: 60
- From 1 Mar 2024 to the primary completion date, 1 May 2025
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- epilepsy or treatment with antipsychotics
- abuse of alcohol or drugs
- previous surgery distorting the anatomy of the sternum, thorax or upper abdominal area
- severe organ dysfunction ( kidney, liver and other); patients who fail at weaning after 12 hours of surgery.
Other illness
- a history of neurological deficits or neuropathy affecting the thoracal innervation
- infection at the site of block application
- allergy to local anesthetics
Other
- refusal to participate
Who the study is looking for
- patients who will undergo CABG surgery with sternotomy
- patients who have an American Society of Anesthesiologists (ASA) Physical Status classification of III to IV
Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Haseki Training and Research Hospital Coordinator of this site? Confirm its status | Istanbul | Turkey (Türkiye) | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.