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NCT05719948

Combined Continuous and Pulsed Radiofrequency Ablation for Pain Relief and Their Safety in Cervical Facet Pain

Completed NA Last updated 15 February 2023
What this trial tests

NA trial testing Flouroscopic guidance cervical medial branch radiofrequency ablation in Radiofrequency Ablation in 43 participants. Completed in 1 February 2023.

Timeline
1 October 2020
Primary endpoint
1 February 2023
1 February 2023

Quick facts

Lead sponsorFayoum University Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingdouble
Primary purposetreatment
Enrollment43
Start date1 October 2020
Primary completion1 February 2023
Estimated completion1 February 2023
Sites1 location across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Fayoum University Hospital

Who can join

Adults 30 to 75, any sex, with Radiofrequency Ablation. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Continuous radiofrequency ablation (CRF) is the effective management for cervical facet joint pain but related with neuropathic symptoms in post-radiofrequency period. Additionally, pulse radiofrequency ablation (PRF) provides relief of neuropathic symptoms. However, the effect of CRF followed by PRF has yet to be validated

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Radiofrequency Ablation

Currently open trials in the same condition.

Other Fayoum University Hospital 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/NCT05719948.

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