Pectoral Fascial (PECS) I and II Blocks as Rescue Analgesia in a Patient Undergoing Minimally Invasive Cardiac Surgery.
Suraj Yalamuri, Rebecca Y Klinger, W Michael Bullock...
https://pubmed.ncbi.nlm.nih.gov/29016551/Actively Recruiting
Led by Fayoum University · Updated on 2024-10-15
90
Participants Needed
2
Research Sites
1 weeks
Total Duration
Researchers are evaluating the use of dexmedetomidine added to ropivacaine in bilateral Pectoral nerve PECS block to improve anesthesia duration and postoperative pain relief for patients undergoing cardiac surgery through midline sternotomy. This phase 4, double-blind randomized controlled study aims to compare the effects of this combination with plain ropivacaine and a control group receiving only fentanyl. The PECS block is a less invasive regional analgesic technique that has been successfully applied in various chest wall surgeries. The study involves three groups of 30 patients each one group receives bilateral PECS block with 30 ml of 0.25% ropivacaine plus dexmedetomidine 0.5 mcgkg per side the second group receives 30 ml of 0.25% plain ropivacaine per side and the control group receives no regional anesthesia but continuous intravenous fentanyl at 1 mcgkghr. All patients receive standard anesthesia, including total intravenous anesthesia with fentanyl, midazolam, and rocuronium, followed by paracetamol infusion after surgery. The PECS block is guided by ultrasound and performed in a supine position, with local anesthetic injected between specific muscle layers. Participants will be monitored through pain assessments using the Visual Analog Scale at multiple intervals during the first 24 hours after extubation, duration of mechanical ventilation, total fentanyl consumption, incidence of complications, length of ICU stay, and patient satisfaction measured by a five-item Likert scale. The study includes assessments of hemodynamic stability, blood gases, coagulation time, and drain output before performing the block. The trial will continue until January 2025, with close monitoring post-surgery in the surgical ICU until patients are fully awake and extubated.
CONDITIONS
Dexmedetomidine Ropivacaine Versus Plain Ropivacaine in Bilateral Pectoralis Nerve (PECS) Block
M
mina fam, M.D
M
Mostafa Elhamamsy, M.D
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Fayoum University
Lead Sponsor
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Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Surgery day plus 24 hours postoperative
Participants undergo open heart surgery with anesthesia and are randomly assigned to receive either ropivacaine with dexmedetomidine, plain ropivacaine, or fentanyl only. Bilateral PECS blocks are performed after surgery for pain management.
1 surgical procedure and continuous monitoring during ICU stay
Duration - 24 hours after surgery
Participants are monitored in the ICU with pain assessments and opioid use measured up to 24 hours after surgery to evaluate analgesia and recovery.
Pain assessments at extubation and 3, 6, 12, 18, and 24 hours postoperatively
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
3
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Lead Sponsor