What is iTind?
iTind is a safe and clinically-proven treatment that relieves lower urinary tract symptoms due to an enlarged prostate, or BPH. The treatment reshapes the anatomy of the prostatic urethra, gently creating new channels for urine to flow freely. The treatment is fast, straightforward and has none of the complications associated with prescription medication, surgery or permanent implants. Developed to meet the needs of active patients, the 5-day treatment minimizes downtime and does not compromise sexual function. That means you are back to yourself, and back to your daily routine, in no time at all.
How does iTind work?
The iTind treatment is a simple procedure performed by a urologist either in the hospital or a clinic. The device is placed in the prostatic urethra in a folded configuration. During the 5-day treatment, it expands and exerts gentle pressure at three precise points to create new channels through which urine can flow through the urethra and out of the body. After 5 days, the device is completely removed. The new channels continue to provide long-lasting relief of BPH symptoms.
Step 1
In your doctor’s office you may receive some light sedation and a local anesthetic. A cystoscope is a miniature camera which will be inserted into your urethra to place the iTind device in your prostatic urethra. Once in place you should be able to urinate freely, so there is no need for a catheter and you will be released to go home.
Step 2
During the next 5 to 7 days you may resume most normal activities, depending on how comfortable you feel. The most common side effect reported while the iTind is in place is pressure around the area of the perineum and increased urgency and frequency to urinate. Some patients also experience some light blood in their urine and slight burning when urinating.
Step 3
After 5 to 7 days, your doctor will completely remove the iTind device using a flexible silicone catheter. Then it’s back to work. Back to play. Back to life!
Why choose iTind?
- Rapid symptom relief in the majority of patients
- Preserves sexual function
- Straightforward, outpatient procedure
- Temporary implant removed after 5 to 7 days
- Minimal downtime
- No need for a catheter
- Durable results as demonstrated in clinical studies out to 3 years1,2,3
As with any medical procedure, individual results vary. Men with moderate to severe BPH symptoms are generally good candidates for the procedure. Speak with your doctor to see if the iTind procedure is right for you.
Some patients experience side effects during the procedure, but they are generally only mild to moderate. Side effects, if experienced, include pain or burning with urination, blood in the urine, pelvic pain, an urgent need to urinate and/or the inability to control the urge. Most of these side effects occur during the 5 to 7 day treatment period and resolve once the device is removed.
Frequently Asked Questions
The iTind is a 5 to 7 day treatment to treat lower urinary tract symptoms (LUTS) due to benign prostatic hyperplasia (BPH), or enlarged prostate.
The iTind is inserted into the prostatic urethra in a folded configuration. Over the next 5 to 7 days it slowly expands to gently widen the opening through which urine can flow. After 5 to 7 days the device is completely removed. There is no permanent implant, heat treatments or tissue ablation. No prostate tissue is removed and initial studies have shown that there is no impact on sexual function.
Together with your urologist you will review your symptoms, routine and lifestyle needs. The iTind procedure is a new alternative to prescription drugs or major surgery, and is ideal for sexually active men who want a minimally-invasive treatment that preserves a high quality of life.
Your doctor will insert the iTind device into the prostatic urethra in the hospital or clinic. Typically, no catheter is required and you can usually return home within a few short hours. After 5 to 7 days at home, you will return to your doctor’s office and the iTind device will be completely removed. There may some slight discomfort during the 5 to 7 days, but symptom relief should be quite rapid for most patients. After the device is removed you can return to your daily routine.
Most patients experience only mild to moderate discomfort while the iTind is in place, however patient experience is variable.
The most common side effects experienced are the feeling of pressure in the area of the perineum, an increased frequency and urgency to urinate, light blood in urine, and slight burning upon urination. However, any side effects experienced typically subside once the iTind is removed.
After insertion of the iTind device, you may be kept for a few hours for observation. Upon returning home you may resume most normal activities depending on your personal level of comfort.
Most patients start to experience symptom relief right after the removal. Symptoms typically continue to improve over the following 6 to 12 weeks.
In clinical studies there have been no indications of long-term adverse side effects. Since the iTind device is completely removed after it has done its job to widen the opening at the prostatic urethra, there is no risk of implant migration, encrustation, or tissue overgrowth that could complicate removal. Moreover, there are no obstacles in maintaining a regular prostate screening program, including physical exams or any type of imaging, such as MRI, if needed.
The device positioning helps to ensure that no damage is caused to sperm ducts or sphincters, avoiding risks of sexual dysfunction. Sexual function was preserved among patients treated in the relevant clinical studies.
Durability has been demonstrated out to three years in terms of symptom improvement, urinary flow and quality of life in a significant number of patients. The iTind treatment does not preclude retreatment or other BPH treatments, should they be needed or desired in the future.
If you have had a previous surgical treatment on your prostate, or have a large median lobe, you may not be a candidate for the iTind procedure. Consult with your doctor to determine whether the iTind is right for you.
Clinical data demonstrates three years durability of the first generation TIND and efficacy at 24 months of the second-generation iTind. Both studies demonstrated preservation of sexual function and urinary continence and a very high safety profile.
You can read more about the clinical data here.
Medi-Tate develops and manufactures iTind for the treatment of BPH. The company is based in Israel. Read more about our company. Medi-Tate Ltd. is now part of the Olympus Group. Visit olympusamerica.com
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