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临床试验/NCT00704912
NCT00704912已完成2 期

Treatment of Hyperandrogenism vs. Insulin Resistance in Infertile PCOS Women

Milton S. Hershey Medical Center2 个研究点 分布在 1 个国家目标入组 217 人开始时间: 2008年9月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
217
试验地点
2
主要终点
Live Birth Rate

研究概览

简要总结

The goal of this three-armed randomized controlled trial is to establish the relative roles of treatment of hyperandrogenism versus obesity (as the largest modifiable factor contributing to insulin resistance) in treating infertility and improving pregnancy outcomes among obese PCOS women. The investigators hypothesize that the key to restoring ovulation leading to live birth is to correct hyperandrogenism with oral contraceptive pills, but the key to avoiding later pregnancy complications is to improve insulin sensitivity with weight loss.

详细描述

Polycystic ovary syndrome (PCOS) is the most common cause of anovulatory infertility among women, and women with PCOS are at increased risk for pregnancy complications such as gestational diabetes and pre-eclampsia. Both hyperandrogenism (HA) and obesity exacerbated insulin resistance (IR) are characteristics of the syndrome, and are targets for treatment, but which should be the predominant focus is still unknown. Phase 1 of this study will be a randomized trial of three preconception interventions in infertile women with PCOS. The first arm will be a combined intervention of medication, meal replacements, and lifestyle modification to improve IR. Orlistat is a gastric lipase inhibitor that reduces the absorption of fat contained in a meal by about 30%. The second arm will be the use of a continuous OCP for 4 months to improve HA. Lo-Estrin 1/20 will be used in a continuous method for 4 months to suppress the ovary. The third arm is the combination of both to improve HA an IR. Phase II of this study will involve ovulation induction with clomiphene citrate with hopeful outcome of pregnancy. Finally, Phase III involve following the pregnancies for outcomes and complications.

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
18 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Partner with sperm concentration of >=14 million/mL in at least one ejaculate with motile sperm.
  • Ability to have regular intercourse 2-3 times per week during the ovulation induction phase of study.
  • At least one patent tube and normal uterine cavity as determined by sonohysterogram, hysterosalpingogram, or hysteroscopy/laparoscopy within the last 3 years, or confirmation of a intrauterine pregnancy within the past 2 years.
  • No previous sterilization procedures(vasectomy, tubal ligation) that have been reversed.
  • Wanting to seek pregnancy.
  • Inclusion Criteria:
  • Chronic anovulation or oligomenorrhea defined as intermenstrual periods of >= 45 days or a total of <=8 periods per year.
  • Hyperandrogenism will be an elevated total testosterone >=50 ng/dL.
  • Hirsutism determined by a modified Ferriman-Gallwey Score >
  • PCO on ultrasound (12 or more follicles measuring 2-9 mm in diameter).
  • BMI >=27 to <=
  • Normal EKG to rule out any abnormalities with the heart.

排除标准

  • Current pregnancy.
  • Patients on oral contraceptives, depo progestins, or hormonal implants.
  • Patients with hyperprolactinemia defined as two prolactin levels at least one week apart >30 ng/mL.
  • Patients with known 21-hydroxylase deficiency by a fasting 17-hydroxyprogesterone (17-OHP) level <2 ng/mL and ACTH stimulation test as needed, or other enzyme deficiency.
  • Patients with menopausal FSH levels >20 mIU/mL.
  • Patients with uncorrected thyroid disease (TSH <0.45 mIU/ML or >4.5 mIU/ML).
  • Patients diagnosed with Type1 or Type II diabetes.
  • Patients with liver disease defined as AST or ALT >2 times normal or total bilirubin >2.5 mg/dL.
  • Patients with renal disease defined as BUN >30 mg/dL or serum creatinine >1.4 mg/dL.
  • Patients with significant anemia (Hemoglobin <10 mg/dL).
  • Patients with a history of deep venous thrombosis, pulmonary embolus, or cerebrovascular accident.
  • Patients with known heart disease that is likely to be exacerbated by pregnancy.
  • Patients with a history of , or suspected cervical carcinoma, endometrial carcinoma, or breast carcinoma. A normal PAP smear or reassuring colposcopy based on current ACOG guidelines will be required.
  • Patient with current history of alcohol abuse.
  • Patients enrolled simultaneously into other investigative studies.
  • Patients taking other medications know to affect reproductive function or metabolism.
  • Patients with a suspected adrenal or ovarian tumor secreting androgens.
  • Patients with suspected Cushing's syndrome.
  • Patients who have undergone a bariatric surgery procedure in the recent past (<12 months).
  • Patients with untreated poorly controlled hypertension defined as systolic blood pressure >=150 mm Hg or average diastolic >=100 mm Hg on three measurements obtained 5 minutes apart. If treated, average systolic blood pressure >= 140 mm Hg or average diastolic >= 90 mm Hg.
  • Patients with medical conditions that represent contraindications to orlistat, OCP, clomiphene, and/or pregnancy.
  • Patients currently participating in lifestyle intervention program (Weight Watchers, Atkins Diet, Curves) or lost more than 5% body weight within the last 6 months.

研究组 & 干预措施

Lifestyle intervention

Active Comparator

Orlistat/Meal Replacement/Lifestyle Modification

干预措施: Orlistat/Meal Replacement/Lifestyle Modification (Drug)

Oral Contraceptives (OCP)

Active Comparator

Loestrin 1/20

干预措施: Loestrin 1/20 (Drug)

Lifestyle/OCP Combined

Active Comparator

Combination of treatments

干预措施: Combination of treatments (Drug)

结局指标

主要结局

Live Birth Rate

时间窗: Participants were followed for 4 months of attempted conception and those who conceived were then followed for the duration of their pregnancy, approximately 9 months.

次要结局

  • Prevalence of Metabolic Syndrome(Baseline, 4 months)
  • Ovulation Rate(Up to 4 months)
  • Change in Weight(Baseline, 4 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Richard S. Legro, M.D.

Professor, Obstetrics and Gynecology and Public Health Sciences

Milton S. Hershey Medical Center

研究点 (2)

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