← Eichor
Study identifier: NCT06444919 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Capsaicin in Digital Osteoarthritis Versus Control

Condition: Osteoarthritis Hand · Neuropathic Pain  ·  Sponsor: University Hospital, Clermont-Ferrand

PhasePhase 4
Planned participants120
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The objective of this multicentric, randomized controlled double-blind clinical trial is to demonstrate the efficacy of transdermal application of capsaicin in patients with painful digital osteoarthritis with a neuropathic pain component. Participants will receive either a transdermal patch of capsaicin 179 mg (8%) or the control treatment (capsaicin 0.04%). Researchers will compare the intensity of pain in the fingers at day 60 in the capsaicin 8% group versus capsaicin 0.04% (control arm)

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

Talk to the study team

Lise Laclautre  ·  334.73.754.963  ·  promo_interne_drci@chu-clermontferrand.fr

Always discuss trial participation with your own doctor first.

Locations (4)

CHU de Clermont-FerrandClermont-Ferrand, FranceRecruiting
HCL Hôpital Edouard HerriotLyon, FranceRecruiting
AP-HP Hôpital Saint-AntoineParis, FranceRecruiting
CHU de Saint-EtienneSaint-Etienne, FranceRecruiting

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/NCT06444919