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DESCRIPTION (provided by applicant): 80% of U.S. women use oral contraceptives (OC) for an average duration of 5 years. There is a large gap between lowest expected failure rates of about 1.5% and typical use failure rates of about 7% per year. This gap may be due to incorrect use or to decreased OC effectiveness in population subgroups. Recent reports suggest greater oral contraceptive failure among heavier women, particularly those using the lowest doses. The prevalence of obesity in the U.S. population has recently increased to about 23% in women aged 20-29, peak years for OC use. Obesity is most prevalent among poor and minority women who already experience higher rates of contraceptive failure. During recent decades, the typical OC dose has decreased by about 75%. OC physiology and effectiveness have not been evaluated in obese women.This is a revised proposal in which we propose a double blind randomized clinical trial to include about 100 normal weight women and 100 obese women with normal ovulatory function at baseline; we will randomize these participants to widely used monophasic oral contraceptives (30ugEE/150ug LN or 20ugEE/100ug LN). Participants will undergo evaluation to detect ovarian follicle development and ovulation during OC use; we will use transvaginal sonograms to assess ovaries and endometrium and will measure circulating endogenous hormones (progesterone). Participants will record bleeding and adverse events using a diary. We will use this data to assess whether obese women are at higher risk of oral contraceptive failure than normal weight women due to less ovarian suppression. We will be able to assess differences by weight and by dose and evaluate weight-dose subgroups. We will be able to assess risk of pregnancy based on development of pre-ovulatory follicles and ovulation. This study will have very good power to detect clinically important differences. Results could directly and immediately affect contraceptive practice.
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Weight and body composition changes during oral contraceptive use in obese and normal weight women.
肥胖和正常体重女性在使用口服避孕药期间体重和身体成分发生变化。
DOI: 10.1089/jwh.2012.4241
发表时间: 2014
期刊: Journal of women's health (2002)
影响因子: --
作者: [Mayeda,ElizabethR, Torgal,AnupamaH, Westhoff,CarolynL]
通讯作者: Westhoff,CarolynL
Contraceptive vaginal ring effectiveness is maintained during 6 weeks of use: a prospective study of normal BMI and obese women.
使用 6 周期间避孕阴道环的有效性保持不变:对正常 BMI 和肥胖女性的前瞻性研究。
DOI: 10.1016/j.contraception.2012.12.001
发表时间: 2013
期刊: Contraception
影响因子: 2.9
作者: [Dragoman,Monica, Petrie,Kelsey, Torgal,Anupama, Thomas,Tiffany, Cremers,Serge, Westhoff,CarolynL]
通讯作者: Westhoff,CarolynL
Pharmacokinetics and ovarian suppression during use of a contraceptive vaginal ring in normal-weight and obese women.
正常体重和肥胖女性使用避孕阴道环期间的药代动力学和卵巢抑制。
DOI: 10.1016/j.ajog.2012.04.022
发表时间: 2012
期刊: American journal of obstetrics and gynecology
影响因子: 9.8
作者: [Westhoff,CarolynL, Torgal,AnupamaH, Mayeda,ElizabethRose, Petrie,Kelsey, Thomas,Tiffany, Dragoman,Monica, Cremers,Serge]
通讯作者: Cremers,Serge
CCTN - PHARMACOKINETIC / PHARMACODYNAMIC EVALUATION OF LEVONORGESTREL BUTANOATE FOR FEMALE CONTRACEPTION
CCTN - PHARMACOKINETIC / PHARMACODYNAMIC EVALUATION OF LEVONORGESTREL BUTANOATE FOR FEMALE CONTRACEPTION
CCTN - CONTRACEPTIVE CLINICAL TRIALS NETWORK - CORE - FEMALE
A Prospective, Randomized Study to Compare Effects of Ulipristal Acetate with a Combined Oral Contraceptive on Breast Epithelial Cell Proliferation.
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