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 @ 6:44 PM
Ignite Modification Date:
2025-12-24 @ 6:44 PM
NCT ID:
NCT07079657
Eligibility Criteria:
Inclusion Criteria:
* Men and women aged 18 and over
* Good general health, no relevant previous illnesses
* Presence of an AGA
* Cognitive ability and willingness to give consent (informed consent)
* Be willing and able to attend follow-up visits
Exclusion Criteria:
* Age \< 18 years
* Pregnant or breastfeeding women
* Scarring alopecia, alopecia due to dermatoses (e.g. lichen ruber, lupus erythemodes,...), alopecia due to chemical or physical noxae, and other non-AGAs
* Significant scarring of the region to be treated
* Significant open wounds or lesions in the region to be treated
* Metallic implants in the head region
* Mental illnesses (psychoses, body perception disorders)
* Use of isotretinoin or other retinoids, psychotropic drugs, coumarins or heparins in the last 2 weeks
* Resurfacing (fractional, ablative, non-ablative) of the affected region \< 2 months before and during the study period
* Tendency to excessive scarring
* Lack of informed consent and/or data protection declarations
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT07079657
Study Brief:
Protocol Section:
NCT07079657