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New treatment option for Androgenetic Alopecia (AGA)
Official title Thulium Laser and Growth Factors for Androgenetic Alopecia
ClinicalTrials.gov ID: NCT07079657
What this study is testing
- What it's testing
- Androgenetic alopecia (AGA) is a common cause of hair loss worldwide. It mainly affects the frontal and parietal regions of the scalp in up to 70 % of men and 40 % of women and has a significant negative psychological and emotional impact on those affected.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older
You may be able to join if
- 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
You likely can't join if
- 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...
- 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
See the full eligibility 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
- 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
The study team makes the final eligibility decision.
Where it's taking place
- Hamburg, Free and Hanseatic City of Hamburg, Germany
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Hamburg, Free and Hanseatic City of Hamburg, Germany. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.