🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Writer Login
Latest
Clinical Trials in Turkey / NCT07716943
Starting soon Not applicable

ASPB-PIPB Combination in Cardiac Surgery

NCT07716943 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-07-01
Last updated
2026-07-21

Condition(s) studied

Postoperative PainCardiac SurgeryCardiopulmonary BypassMedian Sternotomy

Investigational drug(s) / intervention(s)

Combined ASPB and PIPBAnterior Serratus Plane Block

Combined ASPB and PIPB: Ultrasound-guided bilateral anterior serratus plane block combined with bilateral pectoral-intercostal plane block performed after induction of general anesthesia and before surgical incision to provide perioperative multimodal analgesia in patients undergoing cardiopulmonary bypass surgery.

Anterior Serratus Plane Block: Ultrasound-guided bilateral anterior serratus plane block performed after induction of general anesthesia and before surgical incision to provide perioperative analgesia in patients undergoing cardiopulmonary bypass surgery.

Study summary

Cardiopulmonary bypass surgery is associated with significant postoperative pain, which may adversely affect respiratory function, delay mobilization, prolong hospital stay, and increase postoperative complications. Within Enhanced Recovery After Surgery (ERAS) protocols, multimodal analgesia and opioid-sparing strategies have become essential components of perioperative care. Ultrasound-guided fascial plane blocks, including the anterior serratus plane block (ASPB) and pectoral-intercostal plane block (PIPB), have emerged as effective and safe regional anesthesia techniques for cardiac surgery, targeting different sensory innervation of the thoracic wall. However, evidence regarding the combined use of these two blocks remains limited. This study aimed to evaluate whether the combination of ASPB and PIPB improves intraoperative and postoperative analgesia, reduces opioid consumption, and enhances postoperative recovery and ERAS outcomes compared with standard analgesic management in patients undergoing cardiopulmonary bypass surgery.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Patients undergoing open heart surgery via median sternotomy by the Cardiovascular Surgery Clinic * Patients over 18 years of age * ASA II-III patients Exclusion Criteria: * \- Patients undergoing emergency or recurrent surgery * Patients with left ventricular ejection fraction \< 30 * Patients who died per-operatively * Patients who do not provide informed consent * Presence of chronic pain * Presence of allergy to local anesthetics * Presence of infection in the area where the block will be performed * Coagulopathy * Pre-existing neurological deficit * Mental retardation * Anatomical deformity

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Sisli etfal research and training hospital Istanbul Turkey (Türkiye)

More Sisli Hamidiye Etfal Training and Research Hospital trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07716943 on ClinicalTrials.gov ↗ ← All trials in Turkey