Cryo NerVe Block Extremity AmputatioN RegIStry for Post Operative and pHantom Limb Pain
Not yet recruiting
- Conditions
- AmputationAmputation of Lower LimbAmputation of Upper LimbAmputation, Limb LossAmputation, Traumatic/SurgeryCryo Analgesia
- Registration Number
- NCT06908538
- Lead Sponsor
- AtriCure, Inc.
- Brief Summary
The goal of this Registry is to see how the device is used when freezing nerves during an amputation procedure.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 2000
Inclusion Criteria
- Patients who have or will have an amputation procedure;
- Patients who are willing and capable of providing informed consent;
- Patients whose age is 18 years or above, or of legal age to give informed consent specific to state and national law.
Exclusion Criteria
- Women of childbearing potential who are, or plan to become, pregnant during the time of the study;
- Other medical, social, or psychological conditions that in the opinion of the Investigator precludes the subject from appropriate consent or adherence to the protocol.
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary Outcome Measure 30 days CryoNerve Block procedural complications
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
Cryoanalgesia molecular mechanisms nerve regeneration phantom limb pain pathways
Cryo nerve block vs. standard analgesia post-amputation pain outcomes NCT06908538
Biomarkers predicting cryoanalgesia response traumatic amputation patients AtriCure device
Cryo nerve block adverse events management strategies amputation surgery complications
Cryoanalgesia combination therapies amputation pain management AtriCure vs. competitor devices