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临床试验/NCT02922348
NCT02922348撤回3 期

Optimal Hormone Replacement for Women With Premature Ovarian Insufficiency

University of Pennsylvania1 个研究点 分布在 1 个国家开始时间: 2016年3月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
撤回
试验地点
1
主要终点
Recruitment

研究概览

简要总结

The investigators intend to establish feasibility/acceptability of a pilot randomized trial comparing hormone replacement therapy (HRT) and combined oral contraceptives (COCs) in women with premature ovarian insufficiency to estimate differences in quality of life (QOL) and serum hormone assays and markers of bone turnover/cardiovascular risk. At baseline, QOL survey will be administered and serum testing performed. Patients then randomized to HRT or COCs. Repeat testing will be performed after 3 and 6 months.

详细描述

Premature ovarian insufficiency (POI) is a term used to describe when a woman's ovaries stop working normally before the natural age of menopause. Early sequelae of POI include vasomotor symptoms, vaginal dryness, mood swings and insomnia due to estrogen deficiency. Long-term sequelae such as loss of bone mineral density and cardiovascular risk carry are considerable concerns. While exogenous estrogen replacement is recommended for the POI patient population, the optimal regimen for replacement is not clear. One approach to hormone replacement therapy (HRT) is to mimic physiologic ovarian function through full replacement doses of estrogen (either orally or transdermally) to reach the typical serum estradiol levels of a menstruating woman (approximately 104 pg/mL per day) with cyclic progestin therapy for endometrial protection. Another approach uses daily combined estrogen-progestin oral contraceptives (COCs), for ease of administration and increased social acceptability. To date, few studies have been performed comparing the two treatment methods in terms of quality of life measures (vasomotor symptoms, bleeding profile, sexual dysfunction, satisfaction with contraception), endocrine function, bone turnover or cardiovascular risk in POI patients. In this proposal, the investigators intend to establish feasibility and acceptability of a pilot randomized controlled trial comparing traditional HRT with COCs in women with POI and to evaluate differences in quality of life measures, hormone assays, bone turnover and cardiovascular risk between treatment arms. The investigators hypothesize that acceptability and feasibility of the pilot trial will be high and that differences will be detected for all measured variables between treatment arms. Demonstration of feasibility and acceptability of this pilot would allow for the pursuit of a larger trial and identification of a superior treatment regimen would have a meaningful impact on the short and long-term care of this patient population.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
14 Years 至 45 Years(Child, Adult)
性别
Female
接受健康志愿者

入选标准

  • Female patients,
  • Between 14-45 years of age
  • Post-menarchal
  • Presence of uterus
  • POI as defined by: change in menstrual function (oligomenorrhea and/or amenorrhea), elevated serum serum follicle stimulating hormone (FSH), low serum estradiol concentrations, or estrogen deficiency symptoms.

排除标准

  • Pregnancy or lactation within previous 3 months
  • Use of hormonal contraception or replacement within previous 3 months
  • Any contraindication to oral contraceptive pills or hormone replacement therapy per the current drug labels. These could include, but are not limited to: history of venous thromboembolism,estrogen-sensitive cancer history, regular cigarette smoking and history of or active liver disease, etc.
  • Patients will be screened for pregnancy with a urine HCG test at time of screening

研究组 & 干预措施

Hormone Replacement Therapy

Experimental

Patient will be given hormones in the form of: transdermal estradiol patch (Climara) 100 mcg/24 hours weekly, progesterone (Prometrium) 200 mg per day for first 12 calendar days of each month (If patients insurance plan does not cover transdermal estradiol, they will be prescribed oral estradiol 2 mg daily. If patients insurance plan does not cover Prometrium, they will be prescribed medroxyprogesterone (Provera) 10 mg per day for first 12 calendar days of each month).

干预措施: Hormone Replacement Therapy (Drug)

Combined Oral Contraceptives

Experimental

Patients will be given hormones in the form of: monophasic combined oral contraceptive containing ethinyl estradiol 0.035 mg and norgestimate 0.25 mg, 1 tablet daily (21 days of active pills and 7 days of inactive pills)

干预措施: Combined Oral Contraceptives (Drug)

结局指标

主要结局

Recruitment

时间窗: 1 year

Patient willingness to participate and be randomized

次要结局

  • Bleeding profile - Bleeding questionnaire(1 year)
  • Hormone Assays - Dehydroepiandrosterone Sulfate (ng/mL)(1 year)
  • Bone Turnover Markers - Serum N-telopeptide of type I collagen (nmol/L)(1 year)
  • Bone Turnover Markers - Serum osteocalcin (ng/mL)(1 year)
  • Cardiovascular Risk Markers - Total cholesterol(1 year)
  • Vasomotor symptoms - Greene Climacteric Scale(1 year)
  • Bleeding profile - Menstrual diary(1 year)
  • Hormone Assays - FSH (mIU/mL)(1 year)
  • Hormone Assays - Estradiol (pg/mL)(1 year)
  • Cardiovascular Risk Markers - Fibrinogen (mg/dL)(1 year)
  • Cardiovascular Risk Markers - Factor VII (%)(1 year)
  • Vasomotor symptoms - Menopausal Vasomotor Symptoms (MVS) survey(1 year)
  • Hormone Assays - Free testosterone (ng/dL)(1 year)
  • Hormone Assays - Thyroid stimulating hormone (U/mL)(1 year)
  • Cardiovascular Risk Markers - Homeostatic model assessment (HOMA) insulin(1 year)
  • Cardiovascular Risk Markers - C-reactive protein (mg/L)(1 year)
  • Sexual dysfunction - Female Sexual Function Index (FSFI)(1 year)
  • Hormone Assays - Anti-mullerian hormone (pmol/l)(1 year)
  • Cardiovascular Risk Markers - Triglycerides (mg/dL)(1 year)
  • Cardiovascular Risk Markers - Lipoprotein a (mg/dL)(1 year)
  • Cardiovascular Risk Markers - Fasting glucose (mg/dL)(1 year)
  • Cardiovascular Risk Markers - Fasting insulin (pmol/L)(1 year)
  • Satisfaction as Contraceptive Method(1 year)
  • Hormone Assays - Sex-hormone binding globulin (nmol/L)(1 year)
  • Hormone Assays - Total testosterone (ng/dL)(1 year)
  • Cardiovascular Risk Markers - Plasma plasminogen activator inhibitor 1 (ng/mL)(1 year)
  • Cardiovascular Risk Markers - Tissue-type plasminogen activator antigen (ng/mL)(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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