Hormone Therapy

5

Review clinical trials related to Hormone Therapy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Quality of Life of Patients Who Have Undergone Bilateral Mastectomy

We therefore aim to determine whether the type of mastectomy (preventive in a high-risk patient or therapeutic in a patient with a history of cancer), as well as the timing (immediate or delayed) and type of breast reconstruction, influence the quality of life and satisfaction of patients who have undergone bilateral mastectomy. The goal of this observational study is thus to measure and compare the quality of life of patients who have undergone bilateral mastectomy using the BREAST-Q questionnaire.

Participants needed: 115
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: University Hospital, GrenobleUpdated: Jul 13, 2026
Eligibility criteria

Female sex [+4]

Individual under guardianship or curatorship, or deprived of liberty [+1]

Status: Not yet recruiting

Comparing Acupuncture vs. Sham Acupuncture for the Management of Hot Flashes in Prostate Cancer Patients Receiving Hormone Therapy

This study is evaluating whether acupuncture may help reduce hot flashes in men receiving hormone therapy for prostate cancer. Hot flashes are a common side effect of androgen deprivation therapy (ADT) and may negatively affect sleep, mood, concentration, daily activities, and overall quality of life. Participants enrolled in this study will receive acupuncture treatment over a defined treatment period. The study will assess changes in hot flash frequency, severity, and quality of life using patient questionnaires and symptom diaries. Participants will complete a daily hot flash diary during selected 7-day assessment periods and quality-of-life questionnaires during study visits. The primary goal of this study is to determine whether acupuncture may improve hot flash symptoms and related quality of life in men undergoing treatment for prostate cancer.

Participants needed: 40
Trial details
Age: 18-99Biological sex: AllType: InterventionalSponsor: University of KentuckyUpdated: May 27, 2026Locations: 1
Eligibility criteria

Patients with history of prostate cancer with currently receiving hormone therap... [+9]

Patients can't travel for acupuncture [+1]

Status: Not yet recruiting

Comparison of Oral Dydrogesterone and Vaginal Progesterone in Menopausal Hormone Therapy

Menopause is a natural stage in a woman's life that can be associated with symptoms such as hot flashes, night sweats, sleep problems, and vaginal dryness. Menopausal hormone therapy is commonly used to relieve these symptoms. In women with an intact uterus, progesterone must be used together with estrogen to protect the lining of the uterus. The purpose of this study is to compare two commonly used progesterone treatment methods in women receiving menopausal hormone therapy. All participants will use transdermal estradiol gel, and they will be randomly assigned to receive either oral dydrogesterone or vaginal micronized progesterone. This prospective randomized controlled study will evaluate the effects of these treatments on endometrial thickness, menopausal symptoms, vaginal health parameters, bleeding patterns, and quality of life over a 12-month follow-up period. The results of this study may help determine the most appropriate progesterone regimen for women undergoing menopausal hormone therapy.

Participants needed: 200
Trial details
Age: 45-60Biological sex: FemaleType: InterventionalSponsor: Sehit Prof. Dr. Ilhan Varank Sancaktepe Training and Research HospitalUpdated: Mar 27, 2026Locations: 1
Eligibility criteria

Women aged 45-60 years [+4]

Unexplained vaginal bleeding [+6]

Status: Recruiting

Hormone Therapy and Angiotensin-Dependent Arterial and Renal Vasoconstriction in Humans

1. to investigate the association between route of administration of exogenous estrogen (transdermal vs. oral) and cardiorenal risk in cisgender (gender identity aligning with sex at birth) and transgender (gender identity not aligning with sex at birth) women. 2. to investigate the association between exogenous testosterone exposure and cardiorenal risk in cisgender (gender identity aligning with sex at birth) and transgender (gender identity not aligning with sex at birth) men.

Participants needed: 200
Trial details
Age: 18-90Biological sex: AllType: ObservationalSponsor: University of CalgaryUpdated: Mar 27, 2025Locations: 1
Eligibility criteria

Age 18 to 90 years [+1]

Cardiovascular disease (symptoms consistent with myocardial ischemia, previously... [+7]

Status: Recruiting

A Randomized Study Comparing the Immune Modulation Effect of Ribociclib, Palbociclib, and Abemaciclib in ER+/HER2- EBC

The 3 FDA-approved CDK4, 6 inhibitors, palbociclib, ribociclib, and abemciclib, all provided progression-free survival benefits when combined with endocrine therapy in advanced ER+/HER2- breast cancer. But, not all of them provided overall survival benefit in the same setting. One of the proposed mechanisms that influence the overall survival difference is from the different influence of the 3 CDK4, 6 inhibitors on tumor microenvironment and/ or immune system. However, there was no head-to-head comparison of the 3 CDK4, 6 inhibitors in the same study. Neoadjuvant therapy provides a window to obtain tissue samples before treatment, during treatment, and after treatment. We aim to compare the immune modulation effects of palbociclib, ribociclib, and abemaciclib with letrozole in neoadjuvant treatment for ER+/HER2- early breast cancer.

Participants needed: 60
Trial details
Phase: Phase 2Age: 20+Biological sex: FemaleType: InterventionalSponsor: National Taiwan University HospitalUpdated: Mar 16, 2023Locations: 2
Eligibility criteria

Female patients aged ≥ 20 years old at the time of informed consent. [+4]

Pregnant or nursing (lactating) women [+3]