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Laser Treatment for Basal Cell Carcinoma
N/A
Waitlist Available
Research Sponsored by Henry Ford Health System
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3-15 months after treatment
Awards & highlights
No Placebo-Only Group
Summary
This trial will study the effect of using a laser to treat basal cell carcinoma under the guidance of imaging modalities.
Who is the study for?
This trial is for adults with a confirmed diagnosis of superficial or nodular basal cell carcinoma (BCC) that's less than 2.0 cm wide. Participants must be willing to have photos taken and follow instructions, or have someone who can do so on their behalf. Pregnant individuals, those needing surgical excision, unable to commit to a full year of follow-up, unwilling to undergo biopsy, or with herpes in the treatment area cannot join.
What is being tested?
The study tests Nd:YAG laser treatment guided by OCT imaging for BCC removal. It aims to improve precision in targeting cancer cells while monitoring clearance through advanced imaging techniques like OCT and RCM. The main goal is complete cancer removal verified by clinical exams and biopsies.
What are the potential side effects?
While not explicitly listed in the provided information, potential side effects may include skin irritation, redness, swelling at the treatment site due to laser exposure; precise side effects will be monitored throughout the trial.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3-15 months after treatment
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3-15 months after treatment
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Clearance by biopsy
Clearance by imaging
Awards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
1Treatment groups
Experimental Treatment
Group I: Treatment of basal cell carcinoma with Nd:YAG laserExperimental Treatment1 Intervention
All enrolled patients will be treated with the Nd:YAG laser for this study as part of the intentional intervention for this study.
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Who is running the clinical trial?
Henry Ford Health SystemLead Sponsor
311 Previous Clinical Trials
2,176,335 Total Patients Enrolled
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Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Treatment of basal cell carcinoma with Nd:YAG laser
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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