Skin Tag Removal Device; A Clinical Study to Determine Outcomes of Treating Adults with Acrochordons (Skin Tags)

This clinical study is being run to see how safe and effective a new, investigational, non-invasive skin tag removal (STR) device is. It’s a low-risk study led by a licensed dermatologist (the Primary Investigator) and managed by a Clinical Research Organization (CRO)

‍

The study will last approximately 30 days and you will be compensated for your time and travel. You will attend at least 1 in-person visit to: 

Center for Dermatology Clinical Research, Inc. 

2557 Mowry Ave., Suites 25 & 34 

Fremont, CA 94538     

‍

Sponsored by

Patrocinado por

Gesponsert von

Gesponsert von

Opdrachtgever:

UK Innovations GP LTD

Participants

Participantes

Teilnehmenden

Deelnemers:

200

People

Personen

Participate by

Participar mediante

Abschlussdatum

Uiterlijke Inschrijving:

August 11, 2025

11.8.2025

11.8.2025

11.8.2025

Study FAQs

Sign Up
Haga clic aquí para participar
Teilnehmen
Klik hier om deel te nemen

Who is the study for? 

You may participate if you:

  • Are 22 years of age or older
  • Are able to understand, speak, and read English
  • Have at least one skin tag (not located around the eye, eyelid or groin area)
  • Have at least one skin tag approximately the size of a pencil eraser
  • Have access to the internet via smartphone

What is expected of me? 

Complete the online study pre-screener; potentially qualified participants will be notified. If you agree to be in this study & meet eligibility, you will be invited to a medical clinic to speak with a licensed dermatologist (called the “Investigator”), who will decide which tag(s)       is/are best for your treatment in the study. Once treated, you will keep an electronic diary via your smartphone for 210 days. You will be asked to take and upload pictures of the treated skin tag(s).

Some of the visits for this study will be in person and some visits will be virtual telephone or video visits. 

‍

  • Visit 1 (Day 1): In-person visit to determine eligibility and place the skin tag band (s). 
  • Visits 2 & 3: virtual visits to review your progress, photos, and discuss your diary entries.
  • Visit 4 (~Day 30): virtual final study visit to answer any questions or concerns. 
  • Unscheduled visit: If the device falls off early, up to 2 in-clinic visits for reapplication, in-clinic visit to remove your skin tag if it has not fallen off by Day 20 (optional), or any other visits requested by you or deemed necessary by the Investigator

‍

What is the benefit for me?

There is a possible direct benefit to you from being in this study: the removal of one or two skin tags. In addition to your personal benefit, if you take part in this study, you may help others in the future who would want to use this device.

‍

Complete questionnaire to get started.

Sign Up
Haga clic aquí para participar
Teilnehmen
Klik hier om deel te nemen

Skin Tag Removal Device; A Clinical Study to Determine Outcomes of Treating Adults with Acrochordons (Skin Tags)

This clinical study is being run to see how safe and effective a new, investigational, non-invasive skin tag removal (STR) device is. It’s a low-risk study led by a licensed dermatologist (the Primary Investigator) and managed by a Clinical Research Organization (CRO)

‍

The study will last approximately 30 days and you will be compensated for your time and travel. You will attend at least 1 in-person visit to: 

Center for Dermatology Clinical Research, Inc. 

2557 Mowry Ave., Suites 25 & 34 

Fremont, CA 94538     

‍

Click here to take part
Haga clic aquí para participar
Teilnehmen
Klik hier om deel te nemen

Study for

Estudio dirigido a

Zielgrupper der Studie

Onderzoek voor:

Adults aged 22+ with one or greater skin tags

Sponsored by

Patrocinado por

Gesponsert von

Opdrachtgever:

UK Innovations GP LTD

Participants

Participantes

Teilnehmenden

Deelnemers:

200

People

Personen

Participate by

Participar mediante

Abschlussdatum

Duur van onderzoek:

August 11, 2025

11.8.2025

11.8.2025

11.8.2025

Who is the study for? 

¿A quién va dirigido el estudio?

Für wen ist die Studie geeignet?

Voor wie is het onderzoek bedoeld?

You may participate if you:

  • Are 22 years of age or older
  • Are able to understand, speak, and read English
  • Have at least one skin tag (not located around the eye, eyelid or groin area)
  • Have at least one skin tag approximately the size of a pencil eraser
  • Have access to the internet via smartphone

What is expected of me? 

¿Qué se espera de mí?

Was wird von mir erwartet?

Wat wordt van mij verwacht?

Complete the online study pre-screener; potentially qualified participants will be notified. If you agree to be in this study & meet eligibility, you will be invited to a medical clinic to speak with a licensed dermatologist (called the “Investigator”), who will decide which tag(s)       is/are best for your treatment in the study. Once treated, you will keep an electronic diary via your smartphone for 210 days. You will be asked to take and upload pictures of the treated skin tag(s).

Some of the visits for this study will be in person and some visits will be virtual telephone or video visits. 

‍

  • Visit 1 (Day 1): In-person visit to determine eligibility and place the skin tag band (s). 
  • Visits 2 & 3: virtual visits to review your progress, photos, and discuss your diary entries.
  • Visit 4 (~Day 30): virtual final study visit to answer any questions or concerns. 
  • Unscheduled visit: If the device falls off early, up to 2 in-clinic visits for reapplication, in-clinic visit to remove your skin tag if it has not fallen off by Day 20 (optional), or any other visits requested by you or deemed necessary by the Investigator

‍

Contact our study team
skintag@lindushealth.com

What is the benefit for me?

¿En qué me beneficia?

Welchen Nutzen habe ich davon?

Wat is het voordeel voor mij?

There is a possible direct benefit to you from being in this study: the removal of one or two skin tags. In addition to your personal benefit, if you take part in this study, you may help others in the future who would want to use this device.

‍

Complete this questionnaire to take part.

Fülle diesen Fragebogen aus, um herauszufinden, ob Du berechtigt bist

Click here to take part
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