← Eichor
Study identifier: NCT07416448 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Neuroma-Associated Pain Management After Combat-Related Trauma in Ukraine

Condition: Pain Management · Quality of Life · Neuroma  ·  Sponsor: Ukrainian Society of Regional Anesthesia and Pain Therapy

PhaseNA
Planned participants50
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This multicenter interventional study in Ukraine is designed to compare the effectiveness of cryoablation and radiofrequency ablation in managing neuroma-associated pain following combat-related trauma. Adult patients with clinically significant neuropathic pain caused by neuromas will be randomly assigned to receive either image-guided cryoablation or radiofrequency ablation of the affected nerve. Cryoablation uses controlled cold temperatures to temporarily disrupt nerve conduction, while radiofrequency ablation uses thermal energy to modulate nerve function. Both interventions are minimally invasive and performed under image guidance. The study will evaluate changes in pain intensity, opioid consumption, functional outcomes, and patient-reported measures at predefined time points following the procedure. This research aims to provide evidence on which intervention is more effective in reducing pain, improving function, and minimizing the need for opioid medications in patients with combat-related neuroma pain.

This description comes directly from the study's public registry record.

Talk to the study team

Maksym Barsa, MD, PhD  ·  +380952074098  ·  maksymbarsa@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Communal enterprise "Yuri Semenyuk Rivne Regional Clinical Hospital" of Rivne Regional CouncilRivne, UkraineRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07416448