Comparing Two Pain Relief Methods After the Nuss Surgery for Chest Wall Deformity in Patients 14 Years and Older
Led by Papa Giovanni XXIII Hospital · Updated on 2026-06-16
50
Participants Needed
1
Research Sites
4 weeks
Total Duration
AI-Summary
What this Trial Is About
This observational ambispective study focuses on pediatric patients undergoing the Nuss procedure for pectus excavatum. It aims to compare the effectiveness of two pain management strategies Earlier Percutaneous Intercostal Cryoneurolysis EPIC alone versus EPIC combined with Phrenic Infiltration as Cryo Adjuvant PhICA. The study investigates whether adding PhICA reduces postoperative pain scores, the need for rescue tramadol, and differences in hospital stay length, time to oral therapy transition, and mobilization timing, along with any side effects.
Patients treated with EPIC alone received preoperative cryoneurolysis 2 to 7 days before surgery, followed by a postoperative systemic analgesia protocol. Those in the combined group received the same treatment plus a phrenic nerve infiltration with low concentration local anesthetic immediately after surgery before awakening. The study compares a retrospective control group EPIC with a prospectively recruited case group PhICA.
Participants had pain levels assessed using the Numeric Rating Scale NRS at regular postoperative intervals up to 7 days after surgery. Researchers monitored tramadol use, medication intake, hospital stay duration, and time to mobilization. The primary outcome is postoperative pain through hospital discharge, with secondary outcomes including mobilization time and length of hospital stay. Monitoring for any complications related to the techniques is also part of the study.
CONDITIONS
Brief Title
Phrenic Infiltration as Cryoanalgesia Adjuvant for Early Postoperative Pain Following the Nuss Procedure
Research Team
S
Stefano Mariconti, MD
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Patients who undergo minimally invasive repair of pectus excavatum at the pediatric surgery department of the referral tertiary center
You will not qualify if you...
Patients who refuse to participate or whose parents refuse to participate in the study
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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Comparing Two Pain Relief Methods After the Nuss Surgery for Chest Wall Deformity in Patients 14 Years and Older
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Published Research Related To This Trial
Effect of Intraoperative Phrenic Nerve Infiltration on Postoperative Ipsilateral Shoulder Pain After Thoracic Surgeries: A Systematic Review and Meta-Analysis of Randomized Controlled Studies.