Prolong™ - Premature Ejaculation Treatment

You don't need a prescription or a note from your doctor or therapist to access the Prolong™ treatment.

It's designed to be an 'Over-The-Counter' solution, which means anyone aged 18 or older can easily purchase and use the Prolong Device for the effective treatment of premature ejaculation as per our first of its kind FDA De Novo classification.

Absolutely.

Our clinical trials encompassed individuals from diverse backgrounds, representing various walks of life. The only common thread among them was the challenge they faced with premature ejaculation.

Our revolutionary patented device and 6 week training program have not only withstood rigorous peer reviews but have also emerged as the unequivocal Gold Standard treatment due to the incredible results.

In contrast to mere 'quick fixes' like delay creams or pills, our device offers an unparalleled permanent solution. What sets it apart even further is its distinction as the sole premature ejaculation treatment granted FDA's prestigious De Novo classification.

A frequently raised and entirely valid question among new users is the distinction between the Prolong™ Device and a conventional vibrator.

What sets the Prolong™ Device apart is its unique role in addressing premature ejaculation.

We invested considerable effort in testing, experimenting with diverse power levels, vibration patterns, and designs.

Following rigorous assessment, we carefully curated the most efficient configuration. Notably, our device's patented design plays a pivotal role in precisely directing and enhancing the impact of vibrations, making it the sole vibratory device tailored to treat premature ejaculation effectively.

An effect size is a statistical calculation that can be used to compare the efficacy of different agents by quantifying the size of the difference between treatments. It is a dimensionless measure of the difference in outcomes under two different treatment interventions. Effect sizes thus inform clinicians about the magnitude of treatment effects.

See more here.

(Prolong measured at 0.8 which is considerably higher than anything else available)

Prolong™ is regulated by different bodies around the world.

In the U.S, it’s regulated by a little federal agency you may have heard of - the FDA (Food and Drug Administration).

Prolong is regulated by the FDA’s Center for Devices and Radiological Health (CDRH), which is responsible for regulating firms who manufacture, repackage, re-label and/or import medical devices sold in the United States.

In order to get clearance to market, we had to provide clinical performance data - AKA, a clinical trial. Independent trials were conducted in accordance with FDA’s Investigational Device Exemption (IDE)7 regulation. (And the results were pretty impressive.)

In Europe, we have an MDR (Medical Device Regulation) and in the United Kingdom, our device is cleared by the MHRA (Medicines & Healthcare Regulatory Agency).

Unlike freely available products that merely bear a CE mark and claim to treat PE, our unique selling proposition (USP) lies in being a clinically proven, rigorously regulated treatment that has undergone extensive years of scientific trials.

We are constantly working around the clock to gain regulatory approval to provide Prolong™ in other markets too.

Permanently.

The Prolong™ Device is a permanent treatment for premature ejaculation and our clinical trials included a follow up with the participants at 3 and 6 months after their initial 6 week training - We're pleased to say that participants were still seeing further increases and improvements in their ELT (Ejaculation latency time).

Consider Prolong™ in the same way you would any other treatment or medication.

Your treatment period lasts for a specific duration, and upon its completion, you may find you no longer require it. Prolong™ follows this same principle. After the six-week program, your treatment is typically concluded, and concerns about premature ejaculation are often resolved.

You have the option to responsibly dispose of the device or retain it in case you decide to embark on another six-week course.

While there's no scientific data to definitively suggest that repeating the treatment will further enhance your Intravaginal Ejaculation Latency Time (IELT), some customer feedback has indicated potential benefits.