Evaluating a new pain management technique for heart surgery patients
Doppler Evaluation of Ultrasound-guided Pectointercostal Fascial Plane Block in Cardiac Surgery
This study is testing a new pain management technique for heart surgery patients to see if it helps them recover better and feel less pain after their operation.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 40 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Antalya Training and Research Hospital Government |
| Locations | 1 site (Antalya, Muratpaşa) |
| Trial ID | NCT06413290 on ClinicalTrials.gov |
What this trial studies
This observational study aims to assess the impact of the pectointercostal fascial plane (PIFP) block on regional hemodynamic parameters in patients undergoing elective cardiac surgery. The PIFP block is an ultrasound-guided technique that is part of a multimodal approach to postoperative pain management, which is crucial for enhancing recovery after surgery. By comparing patients receiving the PIFP block to a control group, the study seeks to determine its effectiveness in reducing pain and improving recovery outcomes. The study highlights the importance of effective pain management in preventing complications such as pulmonary issues and prolonged hospital stays.
Who should consider this trial
Good fit: Ideal candidates include adults over 18 years old scheduled for elective cardiac surgery with an ASA classification of I-III.
Not a fit: Patients with a history of cerebrovascular disease, Alzheimer's disease, mental disorders, or those requiring emergency surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly improve pain management and recovery for patients undergoing cardiac surgery.
How similar studies have performed: Previous studies have shown that ultrasound-guided fascial plane blocks can effectively reduce postoperative pain in various surgical settings, suggesting potential success for this approach in cardiac surgery.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * elective cardiac surgery * over 18 years, adult * American Society of Anaesthesiology (ASA) I-III Exclusion Criteria: * history of cerebrovascular disease * history of Alzheimer's disease * mental disorder * emergency surgery * re-operated due to surgery-related complications * allergy to local anaesthetics * declining to give written informed consent
Where this trial is running
Antalya, Muratpaşa
- University of Health Sciences, Antalya Training and Research Hospital — Antalya, Muratpaşa, Turkey (Recruiting)
Study contacts
- Study coordinator: Arzu Karaveli
- Email: arzukaraveli@hotmail.com
- Phone: +90 2422494400
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.