Study Evaluating the Analgesic Efficacy of Capsaicin 8% Patches in Chronic Coccygodynia.

Recruiting Phase 3 Interventional Study
Coccyx Disorder Neuropathic Pain Coccygodynia
Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
188 (estimated)
Sponsor
Nantes University Hospital · Other
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About This Trial

The primary objective is to demonstrate the analgesic effect at day 60 of 8% capsaicin patch (Qutenza) for the treatment of patients with coccygodyinia.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * \>18 years old at the pre-inclusion visit * Presenting with chronic coccygodynia: pain in the coccygeal region, increased by sitting and or when rising from a sitting position and pain over the last ten days of intensity greater than or equal to four on the eleven-point numeri…
Contacts

Amélie LEVESQUE, MD

+33240083912

amelie.levesque@chu-nantes.fr

CONTACT