Long Term Safety of Preoperative Percutaneous Intercostal Cryoneurolysis
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age14+
SponsorPapa Giovanni XXIII Hospital
About this trial
Follow up of patients who underwent percutaneous cryoneurolysis for pectus excavatum repair (the Nuss procedure) pain management
Eligibility criteria
Qualifiers
Patients who underwent percutaneous cryoneurolysis.
Patients who underwent surgical correction of pectus excavatum according to the Nuss procedure.
Signed informed consent.
Disqualifiers
Refusal to participate in the study
Peripheral nervous system disorders
Age < 14 years
Failure to attend scheduled follow-up visits
Trial design
Treatments tested in this trial
- Self-report Leeds Assessment of Neuropathic Symptoms and Signs (LANSS) Questionnaire - Pediatric Quality of Life Inventory (PedsQL™) Questionnaire - Patient Self-Assessment Sensory Scale
Treatment groups
50 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov