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Recruiting NCT07789340

NCT07789340 Unipolar Versus Bipolar Radiofrequency Ablation in Knee Osteoarthritis Pain

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Clinical Trial Summary
NCT ID NCT07789340
Status Recruiting
Phase —
Sponsor Tanta University
Condition Bipolar Radiofrequency Ablation
Study Type INTERVENTIONAL
Enrollment 64 participants
Start Date 2026-08-29
Primary Completion 2027-06-01

Eligibility & Interventions

Sex All sexes
Min Age 50 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Unipolar radiofrequency ablationBipolar radiofrequency ablation

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 64 participants in total. It began in 2026-08-29 with a primary completion date of 2027-06-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

This study aims to compare the efficacy of unipolar versus bipolar radiofrequency ablation (RFA) in knee osteoarthritis pain.

Eligibility Criteria

Inclusion Criteria: * Age \> 50 years. * Both genders. * Diagnosed with chronic knee osteoarthritis (KOA) according to the American College of Rheumatology (ACR) criteria and confirmed with plain radiography as the gold standard for the diagnosis of KOA. * One chronic KOA pain not responding to other treatments as physiotherapy, oral analgesics, and intraarticular injection with hyaluronic acids or steroids. * Kellgren-Lawrence grade (II-IV). Exclusion Criteria: * Chronic knee pain induced by infection, inflammation, tumors, and fractures. * Prior knee surgery. * Acute knee pain. * Connective tissue diseases. * Neurologic or psychiatric disorders. * Intra-articular knee corticosteroid or hyaluronic acids in the past 3 months. * Anticoagulant medication. * Local infection of the site of intervention. * Cognitive impairment.

Contact & Investigator

Central Contact

Mohammed S Elsharkawy, MD

✉ mselsharkawy@med.tanta.edu.eg

📞 00201148207870

Frequently Asked Questions

Who can join the NCT07789340 clinical trial?

This trial is open to participants of all sexes, aged 50 Years or older, studying Bipolar Radiofrequency Ablation. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT07789340 currently recruiting?

Yes, NCT07789340 is actively recruiting participants. Contact the research team at mselsharkawy@med.tanta.edu.eg for enrollment information.

Where is the NCT07789340 trial being conducted?

This trial is being conducted at Tanta, Egypt.

Who is sponsoring the NCT07789340 clinical trial?

NCT07789340 is sponsored by Tanta University. The trial plans to enroll 64 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology