Here’s a guide to what to expect with your AMT®-RA procedure.
Take the first step, schedule a hassle-free consultation to determine if you’re a candidate for the AMT®-RA procedure Your treatment provider will provide you with the best suitable treatment.
A consultation with a certified AMT®-RA physician near you can be booked as per your convenience. Check the certified physician near you. Your physician will determine whether you are eligible for the AMT®-RA procedure based on your medical history. During your consultation, the perfect solution for your condition will be advised by your physician.
Based on your eligibility, your physician will schedule your procedure and will provide you with a simple pre-procedure checklist you should follow before arriving for the schedule.
Your physician will perform the procedure in his/her clinic without the need to be hospitalized. The procedure is performed under local anesthesia and you will be awake throughout the procedure. The whole procedure lasts for 45 minutes. Everyone has their own sensitivity to discomfort, but most patients do not find the treatment painful.
AMT®-RA procedure is with no downtime, you can return to your home immediately after the procedure. You will be provided with a post-care guideline booklet by the physician which provides you with detailed information about the minimal post-treatment care you need to follow.
IMPORTANT SAFETY INFORMATION EXPAND +
IMPORTANT SAFETY INFORMATION FOR AMT®-RA
Important Information
The content of this Website is intended for informational purposes only and should not be used as a substitute for advice provided by a qualified healthcare professional. The Website serves as a resource platform for clinicians to assist clinics in integrating AMT®-RA into their practice.
AMT®-RA is a procedural protocol developed by orthopedic surgeons, traumatologists & sports medicine specialists for sports rehabilitation & traumatology. This protocol uses a micrografting device Rigenera® Manufactured by HBW a medical device manufacturing company committed to designing and manufacturing medical products of the highest quality. HBW has received ISO13485:2016 certification for the quality management system. This medical device is a regulated healthcare product, which under European regulations bears the CE mark.
Safety Information
AMT®-RA procedure is not for everyone. You should not have the AMT®-RA treatment in areas with metal, electrical, or electronic implants/devices.
Tell your doctor if you have any medical conditions as AMT®-RA should not be used in patients with fever, malignant tumor, hemorrhagic conditions, epilepsy, recent surgical procedure, pulmonary insufficiency, pregnancy, arthritis rheumatoid (positive rheumatoid factor), family-related inflammatory arthritis, hematoma auris (or “cauliflower ear”), other inflammatory general diseases which are not controlled., any autoimmune disease not controlled, ear reconstruction or otoplasty, knee infection or active synovitis, present articular fibrosis, meniscopathy.
AMT®-RA should not be used in patients with Graves’ disease (an autoimmune disorder that causes overactive thyroid), active bleeding disorders, or seizure disorders.
Common side effects may include, but may not be limited to, muscular pain, temporary muscle spasms, temporary joint or tendon pain, and redness at or near the treatment site.
Ask your Healthcare Provider if AMT®-RA is right for you.
Patient Results May Vary.
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