NOLA, Neuwave Medical

Summary

The primary objective of this registry is to compile data that will be analyzed at various timepoints, as it matures, to understand the impact of selected parameters on procedure and patient outcomes. The database will capture data related to (1) Ablation Procedure parameters, (2) Patient parameters, and (3) Healthcare Provider parameters.


Inclusion Criteria

  • Patients who underwent or are scheduled to undergo a microwave ablation of one or more liver lesions with the NEUWAVE Microwave Ablation System per the device's Instructions for Use (IFU).
  • Patients with signed informed consent (or waiver approved by IRB/EC) who are willing to comply with the assessment schedule, and willing to have data included in the database.
  • Patients greater than or equal to 22 years old at the time of informed consent (or waiver approved by IRB/EC).
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Study Location(s)

Beverly

More about this Clinical Trial

Full Title

A Multicenter Observational Registry to Develop Ablation Parameter Guidance for Microwave Liver Ablation of Soft Tissue Lesions

Details
Disease Type/Condition

Other

Principal Investigator

Wachsman, Ashley

Age Group

Adult

Phase

N/A

IRB Number

STUDY00000339

ClinicalTrials.gov ID

NCT04107766

Key Eligibility
ClinicalTrials.gov

Contact
Phone
310-423-6252
Email
clinicaltrials@cshs.org
Want to join the study or
learn more?

Details
Disease Type/Condition

Other

Principal Investigator

Wachsman, Ashley

Age Group

Adult

Phase

N/A

IRB Number

NEU-2017-04

ClinicalTrials.gov ID

NCT04107766

Key Eligibility
ClinicalTrials.gov

Contact
Phone
310-423-6252
Email
clinicaltrials@cshs.org
Want to join the study or
learn more?