Long Term Safety of Preoperative Percutaneous Intercostal Cryoneurolysis
RecruitingNCT07657845
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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)
Follow up of patients who underwent percutaneous cryoneurolysis for pectus excavatum repair (the Nuss procedure) pain management
Study details
- Official title
- Long Term Safety of Preoperative Percutaneous Intercostal Cryoneurolysis: Neuropathic Pain, Quality of Life and Sensory Recovery in a Paediatric Cohort Following Pectus Excavatum Repair
- Conditions
- Cryo Analgesia
- Pectus Surgery
- Interventions
- Diagnostic test: Self-report Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) Questionnaire - Pediatric Quality of Life Inventory (PedsQL™) Questionnaire - Patient Self-Assessment Sensory Scale
- Sponsor
- Papa Giovanni XXIII Hospital
- Start date
- 2025-02-02
- Primary completion
- 2026-06-13
- Sex
- All
- Age range
- from 14 Years
- Results posted
- No results posted in this snapshot
- Countries
- Italy
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patients who underwent percutaneous cryoneurolysis. * Patients who underwent surgical correction of pectus excavatum according to the Nuss procedure. * Signed informed consent. Exclusion Criteria: * Refusal to participate in the study * Peripheral nervous system disorders * Age \< 14 years * Failure to attend scheduled follow-up visits
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT07657845