Pain management technique for patients undergoing minimally invasive cardiac surgery
The Effects of Combined Serratus Anterior Plane Block on Postoperative Acute Pain After Minimally Invasive Cardiac Surgery
This study tests a new pain management technique for patients having minimally invasive heart surgery to see if it helps them recover better and feel less pain after the procedure.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 20 (estimated) |
| Ages | 18 Years to 80 Years |
| Sex | All |
| Sponsor | Ankara City Hospital Bilkent Academic / other |
| Locations | 1 site (Çankaya, Ankara) |
| Trial ID | NCT06326320 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the effectiveness of a combined Serratus Anterior Plane Block (SAPB) for managing postoperative pain in patients undergoing minimally invasive cardiac surgery (MICS). MICS is associated with significant postoperative pain due to thoracic incisions, which can lead to complications if not managed effectively. The trial aims to assess how this pain management technique can improve recovery outcomes, reduce hospital stays, and minimize the risk of pulmonary and cardiovascular complications. Participants will receive the SAPB intervention in conjunction with standard analgesic protocols.
Who should consider this trial
Good fit: Ideal candidates for this study are adults aged 18 to 80 who are scheduled for elective minimally invasive cardiac surgery and have an ASA physical status of I-III.
Not a fit: Patients who may not benefit from this study include those requiring emergency surgery or those with a history of chronic opioid or analgesic use.
Why it matters
Potential benefit: If successful, this approach could significantly enhance postoperative pain control and improve recovery times for patients undergoing minimally invasive cardiac surgery.
How similar studies have performed: Other studies have shown promising results with similar pain management techniques in postoperative settings, indicating potential for success in this approach.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * 18 to 80 years old * American Society of Anesthesiologists (ASA) physical status I-II-III * BMI 18 to 40 kg/m2 * Elective Minimally Invasive Cardiac Surgery (MICS) Exclusion Criteria: * Patient refusing the procedure * Emergency surgery * History of chronic opioid or analgesic used
Where this trial is running
Çankaya, Ankara
- Ankara City Hospital — Çankaya, Ankara, Turkey (Recruiting)
Study contacts
- Study coordinator: Emine Nilgün N Zengin, MD
- Email: nilbavullu@gmail.com
- Phone: +905063370548
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.