ISRCTN46117662已完成不适用
Comparison of the equivalence of ceftriane plus azithromycin or doxycycline for the treatment of pelvic inflammatory disease
Foundation for the Incentive of Research (Fundacao de Incentivo a Pesquisa) (FIPE) (Brazil)0 个研究点目标入组 112 人开始时间: 2006年1月18日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 112
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- Female
入选标准
- •1. A history of pelvic discomfort for a period of 30 days or less
- •2. Findings of pelvic organ tenderness (uterine or adnexal) on bimanual examination
- •3. Leukorrhea and/or mucopurulent cervicitis and/or untreated known positive gonococcal or chlamydial cervicitis
排除标准
- •1. Current pregnancy as demonstrated by beta-Human Chorionic Gonadotrophin (HCG) or ultrasonography
- •2. Inability to tolerate an outpatient oral regimen as demonstrated by the vomiting of eight ounces of water one hour after taking 10 mg of metoclopramide
- •3. Presence of tubo-ovarian abscess, appendicitis or hemorrhagic ovarian cysts confirmed by ultrasound or laparoscopy
- •4. Pelvic pain over 30 days duration
- •5. Allergy to ceftriaxone, azithromycin or doxycycline
- •6. Antimicrobial therapy within seven days of recruitment
- •7. Delivery, abortion or gynecological surgery within 30 days
- •8. Prior hysterectomy or bilateral salpingectomy
- •9. Homelessness
- •11. Abdominal rebound tenderness
研究者
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