Stranica 1 iz 81 rezultatima
There is little information about the perception of experimentally induced extracephalic pain in migraine. This study investigates the associations between mammography-related pain and migraine. A neurologist clinically assessed 630 women aged 40-74 years attending a population-based breast cancer
OBJECTIVE
To evaluate efficacy and side effects of mastalgia treatment with tamoxifen.
METHODS
Women with moderate to severe mastalgia were elected. Age, relation of mastalgia with menses, tamoxifen doses, months of treatment, side effects and pain control with tamoxifen were analyzed for all
OBJECTIVE
To compare the effectiveness and side effects of cabergoline with bromocriptine for the symptomatic treatment of cyclic mastalgia as a part of the premenstrual syndrome.
METHODS
140 women with premenstrual mastalgia were enrolled in this randomised, open-label trial. Two groups were
Outcome studies of the value of reduction mammaplasties have only recently appeared in the literature. Medical directors of insurance companies and managed care plans have been reluctant to pay for reduction mammaplasties, citing the uncertainty of the medical necessity of the procedure. They have
BACKGROUND
Based on the potential risks of post-menopausal hormone therapy (HT) found by the Women's Health Initiative, guidelines for HT now recommend use of the lowest effective dose and shortest treatment duration consistent with individual treatment goals. Current (2003) guidance established by
BACKGROUND
The objective of this study was to compare bleeding patterns of women using a contraceptive combination of 30 mcg ethinylestradiol (EE) and 3 mg drospirenone (DRSP) continuously or cyclically. Menstrual-related symptoms were also evaluated.
METHODS
This open, prospective, randomized study
BACKGROUND
Patients with breast hypertrophy often experience a number of physical symptoms (including intertrigo, painful bra strap grooves, upper and lower back pain, shoulder pain, neck pain, arm pain, numbness or pain in the hands, breast pain, and headaches), as well as psychosocial difficulty.
OBJECTIVE
To conduct a hospital-based survey to assess women's attitude and acceptance towards menopause and hormone replacement therapy (HRT).
METHODS
The authors conducted a survey in women who visited the menopause clinic in 5 university and public hospitals in Bangkok. A group of 615 women who
OBJECTIVE
The primary efficacy and safety of Mircette (brand of desogestrel/ethinyl estradiol and ethinyl estradiol), an oral contraceptive containing 150 microg desogestrel and 20 microg ethinyl estradiol given for 21 days, followed by 2 days of placebo and then 5 days 10 microg ethinyl estradiol,
OBJECTIVE
To assess the tolerability and endometrial effects of vaginal administration of an allopregnanolone gel to postmenopausal women undergoing estrogen therapy.
METHODS
Thirteen postmenopausal women included in the study were divided into two groups and submitted to two consecutive cycles of
OBJECTIVE
To assess the demographic and clinical characteristics and experience of Turkish women treated with depot medroxyprogesterone acetate (DMPA).
METHODS
This prospective clinical study was carried on 9262 subjects, treated with DMPA at Zekai Tahir Burak Women's Health Education and Research
OBJECTIVE
A postmarketing survey was carried out to determine the efficacy and tolerability of Valette (dienogest 2.0 mg and ethinylestradiol 0.03 mg) in routine gynecological practice.
RESULTS
Valette had excellent contraceptive efficacy (unadjusted Pearl index 0.14), with 11 unplanned pregnancies
Changes in body weight and the incidence of estrogen-related side effects with low-dose oral contraceptives (OCs) containing 20 microg ethinyl estradiol (EE) have not been demonstrated in placebo-controlled trials. Two placebo-controlled, randomized trials demonstrated the efficacy of a low-dose OC
Research in the area of oral contraception currently focuses on the development of selective progestogens that combine targeted progestational and antiovulatory activity with a minimal potential for androgenicity. The present dual-center study was conducted to investigate the efficacy, tolerability,