Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 3:36 PM
Ignite Modification Date:
2025-12-24 @ 3:36 PM
NCT ID:
NCT02763592
Eligibility Criteria:
Inclusion Criteria:
* Aged from 18 to 80 years
* Male or female, for women of childbearing potential, a negative pregnancy test
* Patients with PONP following knee surgery
* Patients with neuropathic pain DN4 ≥ 4
* Patients at least 3 months post-surgery
* Patients suffering from at least the allodynic brush-induced mechanical allodynia symptom (DMA) rated as ≥ 5/10 on the numerical scale
* Patient with no localized neuropathic pain symptoms (DN4\<4) on the contralateral knee
* Intact skin besides the scar of surgery (absence of skin disease, skin irritation, inflammation or injury, such as active herpes zoster lesions, atopic dermatitis, wounds) in the area where the medicated plasters will be applied
* Naive from Versatis® treatment
* Treated with stable systemic analgesic and planned to remain stable all over the duration of the study
* Insured by French social security
* Included or agreement to be included in the national register of participants in biomedical research
Exclusion Criteria:
\-
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
80 Years
Study:
NCT02763592
Study Brief:
Protocol Section:
NCT02763592