Pepper patch could soothe teen nerve pain without pills
NCT ID NCT05997979
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a capsaicin 8% patch (made from chili pepper extract) can reduce chronic nerve pain in teenagers aged 12 to 17 who have had pain for over 3 months after surgery or injury. Half the teens get the real patch, the other half get a placebo dressing. Pain levels are checked before treatment and again 4 months later. The goal is to see if the patch offers better pain relief than a dummy treatment.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- capsaicin 8% patch (QUTENZA®)
- What this could lead to
- If it works, this could offer a new, non-drug option to ease chronic nerve pain in teenagers after surgery or injury.
- What could go wrong
- This is a small early-phase trial with only 46 teens, so results may not apply to everyone. The patch can cause skin irritation or burning, and pain relief may not be long-lasting.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
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About 46 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Mar 2024
- Expected to finish
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Jul 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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12 to 17 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Children aged 12 to 17 years (lower age limit of 12 has been chosen to ensure NPSI full filling). * Male or female. * Persistent neuropathic pain more than 3 months after surgery or trauma despite treatment following recommendations. * Neuropathic pain is defined as a DN4 score equal to or greater than 3/7 or 4/10, and localized in a nerve territory explained by the surgery or the trauma. * Treatment, survey and follow up must be realized in an identified investigating center of the study * For patients of childbearing potential: use of an adequate method of contraception\* during the course of the study through 48 hours after the last patch application (girls of childbearing potential must have a negative serum or urine pregnancy test within 7 days prior to the first patch application). * Adequate contraception includes sexual abstinence, progestogen-only oral hormonal contraception, where inhibition of ovulation is not the primary mode of action, male or female condom with or without spermicide, cap, diaphragm or sponge with spermicide, combination of male condom with either cap, diaphragm or sponge with spermicide (double barrier methods) Exclusion Criteria: * Intellectual deficiency not allowing full filling of NPSI. * Insufficient command of the French language to full fill NPSI and other evaluation tools. * Parents' refusal of consent. * Minor patients' opposition. * Underlying neurological disease. * Ongoing neurotoxic treatment. * Already treated by capsaicin. * Cutaneous lesion on pain area. * Patient presenting a pain area on the face, above the hairline of the scalp, and/or in proximity to mucous membranes * Hypersensitivity to the active substance or to any of the excipients listed in section 6.1 of Qutenza SmPC.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
10 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CHU d'Amiens
RECRUITINGAmiens, France
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CHU d'Angers
RECRUITINGAngers, France
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CHU de Bordeaux
RECRUITINGBordeaux, France
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CHU de Brest
RECRUITINGBrest, France
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CHU de Lyon
RECRUITINGLyon, France
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CHU de Marseille
RECRUITINGMarseille, France
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CHU de Montpellier
RECRUITINGMontpellier, France
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CHU de Nantes
RECRUITINGBrest, France
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CHU de Tours
RECRUITINGTours, France
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Institut Gustave Roussy
RECRUITINGVillejuif, France
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