Estradiol and Testosterone Subdermal Implants for Menopause Treatment (ESTIME)

Trial Title: Estradiol and Testosterone Subdermal Implants for Menopause Treatment (ESTIME)

NCT ID: NCT06343870

Condition: Menopause
Testosterone Deficiency
Estrogen Deficiency

Conditions: Official terms:
Methyltestosterone
Testosterone
Testosterone undecanoate
Testosterone enanthate
Testosterone 17 beta-cypionate

Conditions: Keywords:
menopause
estrogen
testosterone

Study type: Interventional

Study phase: Phase 3

Overall status: Not yet recruiting

Study design:

Allocation: Randomized

Intervention model: Parallel Assignment

Intervention model description: Parallel Assignment

Primary purpose: Treatment

Masking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

Intervention:

Intervention type: Drug
Intervention name: testosterone pellet (100 mg)
Description: Intervention arm: Subdermal implant-bioabsorbable testosterone pellet (100 mg of testosterone)
Arm group label: Testosterone

Other name: testosterone subdermal implant

Intervention type: Drug
Intervention name: Placebo
Description: Pellet of cholesterol (placebo)
Arm group label: Placebo

Summary: Estrogen and androgen deficiencies negatively impact the quality of life of women at different stages of life, especially after menopause. New modalities and new therapeutic alternatives have been researched. Parenteral administration of estradiol and testosterone could be effective to treat symptoms secondary to estrogen and androgen deficiencies and minimize these adverse events. This study evaluates the efficiency of subdermal implant-bioabsorbable use in women with menopausal symptoms associated with secondary estrogen and androgen deficiencies in women with natural menopause, premature ovarian failure or surgical menopause due to cervical cancer. Pharmacokinetic, biochemical, metabolic, thromboembolic and hormonal data will be evaluated, as well as the effects on quality of life, menopausal symptoms and sexual function after treatment.

Detailed description: The clinical study will be carried out on 140 women, who will be divided into three groups: (1) postmenopausal women with menopausal and sexual symptoms (n=60); (2) women with premature ovarian failure (n=40); (3) women with cervical cancer undergoing abdominal hysterectomy with bilateral adnexectomy, with menopausal and sexual symptoms (n=40). All participants will answer questionnaires to assess quality of life, menopausal symptoms and sexual function. All participants will undergo general physical and gynecological examinations, as well as hormonal, biochemical, thromboembolic and imaging tests. The study will last six months. The included participants will undergo the following visits: inclusion (post-selection) and 1, 3 and 6 months after implant insertion. For the pharmacokinetic study, blood samples will be collected at the following periods: inclusion (before implant placement) and after 1h, 2h, 3h, 6h and 12h; one week, two weeks and one month after placement, and then monthly until six months after implant insertion, to evaluate serum levels of Luteinizing hormone, Follicle stimulating hormone, estradiol, estrone, total testosterone and sex hormone-binding globulin. Clinical, biochemical, hormonal and therapeutic parameters will be evaluated before placement (inclusion) and after 3 and 6 months. The Mann Whitney test will be applied to evaluate differences between measurements and the chi-square test will be applied to analyze the proportions of improvement between groups before and after treatment.

Criteria for eligibility:
Criteria:
Inclusion Criteria: - menopause time of 2 to 6 years; - Body Mass Index between 25 and 30 kg/m2; - women hysterectomized and ovariectomized due to cervical cancer; - women with premature ovarian failure and under 40 years of age; - active sex life; - absence of severe depression and anxiety, confirmed by evaluation using the Beck (specific for depression) and Beck (specific for anxiety) questionnaires. Exclusion Criteria: - disabling illnesses; - use of medications that inhibit sexual desire; - inability to answer the questionnaires; - altered routine exams and comorbidities: - Severe hypertension with Blood Pressure measurement > 160 x 90 mmHg in two measurements - clinical or subclinical thyroid dysfunction with Thyroid-stimulating hormone > 4 mIU/L - dyslipidemia - fasting triglyceride level > 400 mg/dL - presence of occult blood in feces - hyperprolactinemia (>29ng/mL) - fasting blood glucose > 100 mg/dL - presence of osteopenia or osteoporosis - BIRADS classification greater than or equal to 3 on mammography - presence of endometrial echo > 4mm on transvaginal ultrasound - presence of changes in oncotic colpocytology - diagnosis after psychological screening of moderate to severe anxiety/depression.

Gender: Female

Minimum age: 18 Years

Maximum age: 60 Years

Healthy volunteers: No

Start date: May 31, 2024

Completion date: April 30, 2025

Lead sponsor:
Agency: University of Sao Paulo General Hospital
Agency class: Other

Source: University of Sao Paulo General Hospital

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06343870