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Long Term Safety of Preoperative Percutaneous Intercostal Cryoneurolysis

Study acronym: CRYOFUP
StatusRecruiting
PhaseNot specified
Started
View on ClinicalTrials.gov ↗

Record History

See every version on ClinicalTrials.gov ↗

  1. Primary endpoint(s) modified
    • Interventions: Questionnaire and Physical Exam (Diagnostic Test) to Self-report Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) Questionnaire - Pediatric Quality of Life Inventory (PedsQL™)…
    • Secondary endpoints revised (3)
    • Study title shortened, about 16 words
    v2
  2. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Follow up of patients who underwent percutaneous cryoneurolysis for pectus excavatum repair (the Nuss procedure) pain management
Trial Details
NCT Number NCT07657845
Lead Sponsor Papa Giovanni XXIII Hospital
Conditions
(from sponsor)		 Cryo Analgesia, Pectus Surgery
Related terms Chronic Pain, Neuralgia
Enrollment 50 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov