Black Onyx Medical | SRT-100
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As a physician, it is up to you to make sure your patients have access to and are making the best choices possible when it comes to treating their non-melanoma skin cancer and keloids. To do so, you must be able to present to them a variety of options for treatment and help them choose the best option for their bodies. While you might have several different options to explore with your patients, the odds are that most of them involve cutting into the skin in some way, which is intimidating for patients wanting the easiest, most painless and efficient way to remove their skin cancer or keloids.



The SRT-100™ is an excellent treatment option for patients with the following conditions: Keloid scars Basal cell carcinoma Squamous cell arcinoma Metatypical carcinoma Cutaneous appendage carcinoma Actinic keratosis Kaposi’s sarcoma
The SRT-100™ is comparable to surgery and is 95% plus effective in curing basal and squamous cell skin cancer.
The SRT-100™ is very effective in treating keloids and boasts a cure rate of 90 percent plus.
Depending on the treatment protocol your physician chooses for your particular case, you may need several treatments per week for up to several weeks. Treatments are brief—usually under one minute.
The SRT-100™ is a safe and proven technology that effectively treats non-melanoma skin cancers, keloid scarring, actinic keratosis and Kaposi’s sarcoma. It is utilized by dermatologists and radiation oncologists all over the world because it delivers good patient outcomes.
You should expect the same results as surgery, but with these additional benefits: No pain No anesthesia No cutting No bleeding No stitching No scarring No interruption of lifestyle No reconstructive surgery
The SRT-100™ doesn’t harm surrounding or underlying healthy tissue while targeting cancer cells. The SRT-100™ provides excellent cosmetic outcomes and is a great alternative for patients with various co-morbidities.
No. The SRT-100™ is a non-invasive procedure. Since it does not require incisions, patients are not left with any scarring post-treatment.
Yes, the SRT-100™ has been cleared by the Federal Drug Administration for use on the entire body—making it especially effective in the treatment of non-melanoma skin cancer and keloid scars.
In cases where there are larger possible risks, you may be asked to agree in writing to the doctor’s plan for your care. This is part of informed consent. It recognizes your need to know about a procedure, surgery, or treatment, before you decide whether to have it. It’s common to go through the informed consent process before starting cancer treatment. If you are getting more than one type of treatment, you will likely need separate informed consents for surgery, chemotherapy, and radiation. After your first talk with your doctor, you may have only a general idea of the treatment plan. You’ll likely want to know more so that you can think about the ways this plan may affect your health and your life. In order to freely decide whether the risks are worth the benefits you expect to get from the treatment plan, you must understand the risks and drawbacks of the plan. Most people find that they need to get some questions answered before they can decide on a treatment plan that carries some risk for them. Informed consent is a process that includes all of these steps: You are told (or get information in some way) about the possible risks and benefits of the treatment. You are told about the risks and benefits of other options, including not getting treatment. You have the chance to ask questions and get them answered to your satisfaction. You have had time (if needed) to discuss the plan with family or advisors. You are able to use the information to make a decision that you think is in your own best interest. You share your decision with your doctor or treatment team. If you have gone through these steps and decide to agree to the treatment or procedure, you are usually asked to sign a paper called a consent form. The completed and signed consent form is a legal document that lets your doctor go ahead with the treatment plan. The consent form names the procedure or treatment to be done. The rest of the form may be very general, stating only that you have been told about the risks of the treatment and other available options. Or it may be very detailed, outlining what the risks and other options are. Depending on how it’s presented, you may sign for one certain procedure or treatment, or you may give blanket approval for any treatments and procedures that the health provider decides are needed. From the doctor’s viewpoint, informed consent means: A doctor or nurse must make every effort to be sure the patient understands the purpose, benefits, risks, and other options of the test or treatment. Then the doctor or nurse must get the patient’s consent before starting. In some cases, even a simple blood test or an injection (“shot”) requires written consent from the patient. As long as adult patients are mentally able to make their own decisions, medical care cannot begin unless they give informed consent. If the patient is a minor (under age), has a serious mental disability, or cannot give consent, then the parent, legal guardian, or a person authorized by the court must give consent before treatment can start. This is usually a close family member who has reason to know what the patient would want. (See “Who besides the patient can give consent?” in the section “What are the legal requirements of informed consent?”) As some very public court cases have shown, an elaborate legal system is in place to guide cases in which the patient is mentally or physically unable to give informed consent for treatment. These cases have come up when the patient is in a coma (unconscious) or on life support. Sometimes health care workers refer to the consent form itself as an “informed consent.” This is not quite accurate. Informed consent is the process and actions that take place as you learn about and think about a treatment before you agree to it. Your signature on the form is taken to be evidence that this took place. If you decide that you do not want the procedure or treatment, you should not sign the consent form. In this case, you may be asked to sign an informed refusal form or a form that states you are choosing not to follow medical advice. Your signature on this form implies that you know the risks of refusing, so be sure that you understand these risks and know your other options before you sign.