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Cryoanalgesia to Prevent Acute and Chronic Pain Following Nuss Procedure

CompletedNot applicableNCT05570097
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

This Study study compared standard therapy (multimodal and regional analgesia) versus a novel approach (Cryoanalgesia combined with bilateral erector spine plane block and multimodal analgesia) in subjects undergoing minimal invasive modyfied Nuss procedure (thoracoscopy).

Study details

Official title
Cryoanalgesia in Combination With the Novel Prehabilitation Program Back on Feet Are the Essential Parts of Enhanced Recovery Protocol in the Minimal Invasive Modyfied Nuss Procedure of Children With Funnel Chest Deformation.
Conditions
  • Funnel Chest
  • Excavatum, Pectus
Interventions
  • Device: intercostal nerves cryoanalgesia
Sponsor
Pomeranian Medical University Szczecin
Start date
2022-09-28
Primary completion
2022-10-10
Sex
All
Age range
from 10 Years
Results posted
No results posted in this snapshot
Countries
Poland
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patients undergoing pectus excavatum repair with modyfied minimal invasive thoracoscopic NUSS technique * aged 10 years or above 10 * informed consent signed for cryoanalgesia Exclusion Criteria: * Age of 9 years or below * Refuse to receive cryoanalgesia or regional analgesia as primary pain relief * Any contraindication to cryoanalgesia * Difficult follow-up for geographical reasons and/or impossibility by the patient to understand how to perform self-measurements

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT05570097