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NCT03658018: CLBP

Intraosseous Basivertebral Nerve Ablation for Treatment of Chronic Low Back Pain

Withdrawn NA Last updated 15 August 2019
What this trial tests

NA trial testing Intracept System Ablation in Chronic Low Back Pain. Withdrawn.

Timeline
2 January 2019
Primary endpoint
12 July 2019
12 July 2020

Quick facts

Lead sponsorRelievant Medsystems, Inc.
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Start date2 January 2019
Primary completion12 July 2019
Estimated completion12 July 2020
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Relievant Medsystems, Inc.

Who can join

Adults 25 to 70, any sex, with Chronic Low Back Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Objective of study is to evaluate the procedural success rate, clinical effectiveness, and heath-economic profile using the Intercept Intraosseous Nerve Ablation System in adult subjects with chronic low back pain in the post-market setting

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of Intracept System Ablation

Trials testing the same drug.

Other recruiting trials for Chronic Low Back Pain

Currently open trials in the same condition.

Other Relievant Medsystems, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03658018.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing