Radiofrequency Plus Superficial Cervical Plexus Block in Treatment of Cervical Spondylosis Pain
Comparative Study Between Cervical Medial Branch Radiofrequency Ablation Versus Radiofrequency Plus Superficial Cervical Plexus Block in Treatment of the Cervical Facet and Cervical Spondylosis Pain
Ain Shams University
53 participants
Jun 20, 2024
INTERVENTIONAL
Conditions
Summary
The goal of this clinical trial is to compare the effectiveness in the pain relief between doing radiofrequency ablation for the medial branch of the cervical facet pain alone vs using it combined with superficial cervical plexus block.in adults patients with cervical spondylosis pain The main question it aims to answer is: does adding superficial cervical plexus block to radiofrequency in patients with chronic neck pain provide better analgesia than radioprequency alone ?
Eligibility
Inclusion Criteria5
- Both genders.
- Age between 30-70 years.
- American society of anesthesiologist ASA 1,2 \& 3 physical status.
- MRI cervical spine diagnosing cervical facet arthropathy originating pain .
- Failed full dose medical treatment and life style modification and physiotherapy for 3 months prior to intervention.
Exclusion Criteria10
- Neurological disorders.(previous central and peripheral CNS affection ).
- coagulopathy INR \> 1.8 or platelets \< 50,000.
- Infection at or near the injection site.
- Presence of pacemaker or defibrillator.
- known allergy to used medications.
- age \>70 or \<30 years.
- patients with previous history of Radiotherapy , chemotherapy or metastasis
- pregnant patients.
- patients with rheumatological disorders ( rheumatoid arthritis, diffuse idiopathic skeletal hyerostosis, psoriatic arthritis, spondyloarthritis)
- patients with antiphospholipid syndtrome.
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Interventions
patients will receive cervical radiofrequency ablation on both sides then after 2 weeks they will be readmitted and will receive superficial cervical plexus block on one side only
Locations(1)
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NCT06480175