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A Safe and Effective Solution for More Women

Unlike older endometrial ablation methods that have strict patient exclusions, Minitouch is designed to treat a broader range of women, including those who are traditionally considered high-risk or ineligible for other procedures.

With its gentle, low-temperature energy delivery and no need for general anesthesia, Minitouch offers consistent, excellent outcomes for a diverse patient population.

Same Excellent Outcomes Regardless of Covariates

Clinical studies show that Minitouch delivers equally successful outcomes across a variety of patient backgrounds, including:

94% of patients experienced a significant reduction in bleeding, and 95% reported a reduction in period pain—with no difference in success rates based on patient history or uterine variations.

Patients with prior C-sections

Women with larger or irregular uterine cavities

Patients with fibroids that do not distort the cavity

Women of all BMI categories

A Solution for Patients Contraindicated for General Anesthesia or IV Sedation

Many women cannot or prefer not to undergo general anesthesia or IV sedation, making them ineligible for traditional ablation methods. Minitouch eliminates this barrier by providing:

01

A completely in-office procedure

no hospital stay required

02

A gentle experience without IV sedation

reducing risks for high-risk patients

03

A safer alternative for women with anesthesia

sensitivities or medical contraindications

This means more women can access a long-term solution for heavy periods, without the risks associated with surgery or aggressive ablation techniques.

Minitouch provides a safe, effective treatment option

for more women, including those who cannot tolerate anesthesia or other invasive procedures.