Percutaneous Intercostal Cryoneuromodulation Onset Timing.
Recruiting
Observational Study
Cryotherapy Effect
Pectus Excavatum
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Healthy Volunteers Welcome
You do not need to have the condition being studied to take part.
No Study Drug
Researchers observe your health over time — no experimental treatment is given.
At a Glance
- Age
- 12 – 40
- Sex
- Any
- Study type
- Observational
- Participants needed
- 20 (estimated)
- Sponsor
- Papa Giovanni XXIII Hospital · Other
Who this trial is looking for
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Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
Percutaneous Intercostal Cryoneurolysis is a promising technique that addresses acute postoperative pain after Nuss procedure for pectus excavatum. However its onset timing has not yet been determined. A physical examination would assess the variation of chest skin sensitivity to soft touch, cold (water at 4°C), and heat (water at 40°C) through days following the cryoneurolysis procedure.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients who are undergoing preoperative percutaneous intercostal cryoneurolysis for pectus excavatum surgery
Exclusion Criteria:
* failure to obtain consent
Inclusion Criteria:
* Patients who are undergoing preoperative percutaneous intercostal cryoneurolysis for pectus excavatum surgery
Exclusion Criteria:
* failure to obtain consent