Estimation of the Localization Accuracy of the Genicular Ablation Procedure Applied for Chronic Pain Suppression
NCT ID: NCT02873611
Last Updated: 2016-08-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
30 participants
INTERVENTIONAL
2016-08-31
2017-08-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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MRI scanning and the genicular ablation
patients undergoing both MRI scanning and the genicular ablation procedure. additional MRI testing of apprx. 0.5-1 hour
MRI
patients will undergo an additional MRI testing of apprx. 0.5-1 hour.
genicular ablation procedure
Interventions
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MRI
patients will undergo an additional MRI testing of apprx. 0.5-1 hour.
genicular ablation procedure
Eligibility Criteria
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Inclusion Criteria
* Diagnosed with primary degenerative osteoarthritis.
* Complaining of knee pains
* Patients clinically eligible for genicular nerve ablation procedure non-electively based on physical examination
* Patient signed ICF
Exclusion Criteria
* Claustrophobic or failing cooperativity assessment of laying still during long MRI scans
* Pregnancy or pregnancy suspicion
* Enrolled in concurrent studies that may confound the results of this study
* Clinical condition that in the investigator's opinion would not allow the subject to complete the study, e.g., tremor, extreme obesity, mental disorders.
18 Years
80 Years
ALL
No
Sponsors
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TPM Medical Systems Ltd.
INDUSTRY
Responsible Party
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Principal Investigators
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Yehuda Fridman, MD
Role: PRINCIPAL_INVESTIGATOR
Assuta MC
Central Contacts
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Other Identifiers
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CL-001-F1
Identifier Type: -
Identifier Source: org_study_id
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