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NCT Number: NCT07260825

Use of Topical Testosterone and Estrogen vs Estrogen Alone in Vulvodynia: a Randomized Controlled Trial

We are looking to see if patients using both topical testosterone and estrogen will have a greater improvement in pain with vaginal penetration compared to those using topical estrogen alone.

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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

Cincinnati Urogynecology Associates, Cincinnati, Ohio, United States

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About this study

You are being asked to take part in this research study because you have vulvodynia. Vulvodynia refers to pain in the female vestibule. The vestibule is the area that encircles the vaginal opening and the urethra opening. One of the symptoms of vulvodynia is pain with intercourse.

The purpose of this research study is to determine if using estrogen cream versus a combined cream with estrogen and testosterone helps decrease your pain with intercourse.

Multiple studies have been conducted looking at the use of combined cream with estrogen and testosterone to treat vulvodynia. However, none of the studies have compared this to using estrogen cream alone. It is well known that estrogen cream applied to the vagina helps reduce symptoms of vulvodynia. Combined creams with estrogen and testosterone have been shown to help patients who have vulvodynia and are taking birth control pills.

In 2016, the FDA approved a vaginal cream, known as DHEA, to help women with painful intercourse. This is a substance that once applied to the vagina, turns into a mixture of estrogen and testosterone. We know from prior research that the vestibule area is rich in testosterone receptors, so it makes sense that DHEA cream applied vaginally would be able to help vulvodynia patients. However, we do not know the ratio of the breakdown of estrogen versus testosterone from the DHEA substance.

Testosterone applied to the vagina has been shown to improve symptoms in patients with other vulvar conditions, such as lichen sclerosus. Lichen sclerosus is a chronic skin condition that primarily affects the genital area, but it can also affect other areas of the body. It is characterized by white, thickened patches of skin that may be itchy, sore, or painful.

Although topical DHEA was FDA approved for use in women with painful intercourse in 2016, topical testosterone combined with estrogen is not FDA approved for use in women, which means it is investigational. However, it is becoming more common as a treatment option for patients with vulvodynia, and its safety and effectiveness in women has been demonstrated in other studies.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 18 years or older
  • Patients with vulvodynia who present with pain (with vaginal penetration) rating score of 4 or greater

Exclusion criteria

  • Active vaginal infection
  • Pregnancy
  • Breast-feeding
  • Taking anti-androgenic medication (finasteride, dutasteride)
  • Using any other topical hormones to the vulva or vagina

Treatment and study plan

Estradiol 0.01% Vag Cream

Drug

0.01% Estradiol cream, 1g to be applied to the vestibule twice daily for 12 weeks

testosterone 0.1% and estradiol 0.01% vaginal cream

Drug

0.01% Estradiol and 0.1% testosterone cream, apply 1g to the vestibule twice daily for 12 weeks

Primary outcomes

  1. Typical pain with vaginal penetration within last 2 weeks

    Time frame: at 12 weeks post-treatment

    Typical pain with vaginal penetration within last 2 weeks using numeric rating scale

Secondary outcomes

  1. Typical pain with vaginal penetration within last 2 weeks

    Time frame: at 6 weeks post-treatment

    Typical pain with vaginal penetration within last 2 weeks using numeric rating scale

  2. Sexual function

    Time frame: at 6 weeks and 12 weeks post-treatment

    sexual function as measured by Female Sexual Function Index

  3. Most intense pain with vaginal penetration within last 2 weeks

    Time frame: at 6 weeks and 12 weeks post-treatment

    Most intense pain with vaginal penetration within last 2 weeks using numeric rating scale

Study contacts

Contact information is provided by the study sponsor or research team.

Gisele Moran, MD, MPH

CONTACT

[email protected]

513-463-4300

Sponsors and collaborators

Lead sponsor

TriHealth Inc.

Other

Registry information

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Dec 3, 2025
Registry last updated
Dec 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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