Observational Study of the Use of 8% Capsaicin Patch in Children 0 to 18 Years

Status: Recruiting
Location: See all (20) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

Patients aged less than 18-y with validated 8% capsaicin patch treatment in routine healthcare will be offered to participate the study. If they accept it as well as their parents, they will be included in the study . Medical data will be recorded and at home, the child or his family will collect pain assessment data. Tolerance will be monitored at home by phone call from investigational team every 24 hours until normalization. (Less than 24 hours for 75%, 100% to 72 hours on unpublished personal series.) Children will be assessed via scales at inclusion and 1-month, 3-month and 6-month.

Eligibility
Participation Requirements
Sex: All
Maximum Age: 17
Healthy Volunteers: f
View:

• chronic localized neuropathic pain

• capsaicin 8% patch treatment indication validated in a pediatric chronic pain center

• agreement for participation by child and parents

Locations
Other Locations
France
CHU d'Amiens
NOT_YET_RECRUITING
Amiens
CHU Angers
NOT_YET_RECRUITING
Angers
CHU Bordeaux
RECRUITING
Bordeaux
CHR Bourg en Bresse
NOT_YET_RECRUITING
Bourg-en-bresse
CHU de Brest
RECRUITING
Brest
CHU Caen
RECRUITING
Caen
CHU Grenoble
NOT_YET_RECRUITING
Grenoble
CHU Lille
RECRUITING
Lille
CHU Limoges
NOT_YET_RECRUITING
Limoges
CHU Lyon
RECRUITING
Lyon
CHU Marseille
RECRUITING
Marseille
CHU Montpellier
RECRUITING
Montpellier
CHU Nancy
NOT_YET_RECRUITING
Nancy
CHU Nantes
RECRUITING
Nantes
CHU Robert Debré
NOT_YET_RECRUITING
Paris
CHU Trousseau
NOT_YET_RECRUITING
Paris
CHU Rouen
RECRUITING
Rouen
CHRU Strasbourg
RECRUITING
Strasbourg
CHU Toulouse
RECRUITING
Toulouse
Institut Gustave Roussy
RECRUITING
Villejuif
Contact Information
Primary
Philippe J Le Moine, MD
philippe.lemoine@chu-brest.fr
+33298223956
Time Frame
Start Date: 2022-05-12
Estimated Completion Date: 2027-09-12
Participants
Target number of participants: 160
Related Therapeutic Areas
Sponsors
Collaborators: Fondation Apicil, Fondation de France
Leads: University Hospital, Brest

This content was sourced from clinicaltrials.gov

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