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Estetrol for the Treatment of Female Sexual Arousal Disorder in Postmenopausal Women

E

Estetra

Status and phase

Active, not recruiting
Phase 2

Conditions

Sexual Dysfunction, Physiological

Treatments

Drug: 20 mg estetrol monohydrate
Other: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT06308614
MIT-Do001-C206

Details and patient eligibility

About

The goal of this clinical trial is investigating estetrol (E4) in women after menopause, suffering from sexual arousal disorder. The main question it aims to answer is: is 20 mg estetrol monohydrate effective in the treatment of sexual arousal disorder in women after their menopause. Participants will visit the clinic 7 times and complete a daily diary while receiving estetrol or placebo for 12 weeks. Placebo is a pill that looks the same as estetrol but has no active ingredient. Researchers will compare estetrol and placebo to see if estetrol has an effect on the sexual arousal of the participants.

Enrollment

82 patients

Sex

Female

Ages

40 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Main Inclusion Criteria:

  • Hysterectomized postmenopausal women, ≥40 up to ≤65 years, diagnosed with Female Sexual Arousal Disorder

Main Exclusion Criteria:

  • Not willing to stop any hormonal products during their participation in the study
  • History of unresolved sexual trauma or abuse that is contributing to any sexual dysfunction problem
  • Have experienced a recent major life stress or relationship discord that could interfere with sexual activity
  • Clinically significant abnormal gynecological findings
  • History of malignancy, with the exception of basal cell or squamous cell carcinoma of the skin
  • Systolic BP higher than 140 mmHg, diastolic BP higher than 90 mmHg
  • Is judged by the investigator to be unsuitable for any reason

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

82 participants in 2 patient groups, including a placebo group

Estetrol
Experimental group
Description:
20 mg estetrol monohydrate
Treatment:
Drug: 20 mg estetrol monohydrate
Placebo
Placebo Comparator group
Description:
Matching Placebo
Treatment:
Other: Placebo

Trial contacts and locations

24

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Central trial contact

Clinical Study Leader

Data sourced from clinicaltrials.gov

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