Estimation of the Localization Accuracy of the Genicular Ablation Procedure Applied for Chronic Pain Suppression

NCT02873611 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2016-08-19

No results posted yet for this study

Summary

Estimation of the localization accuracy of the genicular ablation procedure applied for chronic pain suppression

Conditions

Interventions

DEVICE

MRI

patients will undergo an additional MRI testing of apprx. 0.5-1 hour.

PROCEDURE

genicular ablation procedure

Sponsors & Collaborators

  • TPM Medical Systems Ltd.

    lead INDUSTRY

Principal Investigators

  • Yehuda Fridman, MD · Assuta MC

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-08-31
Primary Completion
2017-08-31
Completion
2017-08-31

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02873611 on ClinicalTrials.gov