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:
2025-12-25 @ 12:06 AM
Ignite Modification Date:
2025-12-25 @ 12:06 AM
NCT ID:
NCT04259658
Eligibility Criteria:
Inclusion Criteria:
* Trial subject must be able to understand the participant information.
* Histologically verified cutaneous or subcutaneous, primary or secondary cancer of any histology.
* The patient can undergo any simultaneous medical treatment (endocrine therapy, chemotherapy, immunotherapy etc.).
* The patient can undergo radiation therapy during the study period, provided that the treatment field does not involve the treated area.
* Performance status ECOG/WHO ≤2
* At least one cutaneous or subcutaneous tumour measuring at least 5 mm.
* Both men and women who are sexually active must use safe contraception (contraceptive coil, deposit injection of gestagen, subdermal implantation, hormonal vaginal ring or transdermal patch.)
* Signed informed consent.
Exclusion Criteria:
* Pregnancy or lactation
* Allergy to local anaesthesia
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT04259658
Study Brief:
Protocol Section:
NCT04259658