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Request for Minerva Product Trial

Request for Minerva Product Trial

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Started by Ford Williams 7 years, 7 months ago

Request for Product Trial

Procedure Description:

Minerva is the first entirely new endometrial ablation technology introduced in the last 17 years and uses a novel mechanism of action, plasma thermal conduction, over a two-minute treatment cycle to ablate the lining of the endometrium.

Advantages:

Patient Safety

Proprietary safety features include:

  • visual confirmation of cervical seal prior to safety check
  • CO2 extension tubes designed for greater sensitivity in detecting perforations
  • maximum 40 watts of energy delivery modulated by real time impedance monitoring vs maximum 180 watts of constant power delivery

Efficacy

In comparison to the nearest competitor, Minerva demonstrated the following in FDA trials:

  • highest amenorrhea rate – 72% vs 36%
  • highest long term success rate – 93% vs 76%
  • lowest long term hysterectomy rate – 0.91% (1 total) vs 6.3% (11 total)
  • more effectively treats patients with a uterine sounding length greater than 6 cm

Ease of Use

  • silicone array which inserts and removes easily
  • intracervical sealing balloon
  • visual touchscreen interface

We the undersigned wish to trial the Minerva endometrial ablation system for the reasons stated above.

5 Comments

A
Anonymous
7 years ago Featured

I have used this device multiple times over the last 2 years with great results and ease of use.

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Sarah Warner
7 years ago Featured

we really need this tech in our OR, the outcomes for the patients look way better than what we have now

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Christi Hunt
7 years ago

Minerva is my primary choice for endometrial ablation

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Michelle Simmons
7 years ago

I fully support using Minerva at Mission

S
Stacey Olney
7 years ago

I support using the Minerva ablation device in the Mission OR/ASC

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