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临床试验/NCT03398811
NCT03398811已完成不适用

Predictors of Abnormal Uterine Bleeding in Progestin-only Contraceptives Users

Assiut University1 个研究点 分布在 1 个国家目标入组 390 人开始时间: 2018年8月1日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
已完成
入组人数
390
试验地点
1
主要终点
Number of women developed vaginal bleeding

研究概览

简要总结

The use of progestin-only methods of contraception has been increased obviously and progressively over the world in the last few years. Progestin-only contraception is an option for women in whom an estrogen-containing contraceptive is either contraindicated or causes additional health concerns.

Progestogen-only pills are contraceptive pills that contain only synthetic progestogens (progestins) and do not contain estrogen . The progestin-only pill is recommended over regular birth control pills for women who are breastfeeding because the mini-pill does not affect milk production.

The most common progestin-only method used is the injectable depot medroxy-progesterone acetate which had been approved by Food and Drug Administration since 1992 . depot medroxy-progesterone acetate provides reliable, private, long-acting (three months) and reversible contraception. Users of depot medroxy-progesterone acetate don't need daily taking as well as it doesn't affect the intercourse by any mean.

The etonogestrel implant (Implanon) is a single-rod progestin contraceptive method placed subdermally in the inner aspect of upper non dependant arm for three years. Much evidence supports the safety, efficacy, reversibility and acceptability of this contraceptive method.

A common reason women choose to discontinue progestin-only contraception is dissatisfaction with its effects on uterine bleeding which occurs in a significant number of users. Information revealed from many clinical trials shows that abnormal uterine bleeding with progestin-only contraception ranging from 10 to 25 % at first year of use.

研究设计

研究类型
Observational
观察模型
Case Only
时间视角
Cross Sectional

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

  • Women aged between 18-40 years.
  • Women with more than 12 month postpartum.
  • Women who had normal menstrual pattern (cycle from 21 - 35 days with a same cycle length variation of no more than 5 days, bleeding days from 2-7 days and number of sanitary pads not more than 3 pads without blood clots or flooding of blood).
  • Women wanted to use DMPA, etonogestrel subdermal implant or POPs only for pregnancy prevention for at least 1 year.

排除标准

  • Women on any anticoagulant therapy.
  • Women who had a history of uterine, cervical or ovarian pathology.
  • Women who had uterine bleeding disturbance (including amenorrhea) before recruitment.
  • Women received DMPA injection within the previous 9 months except they had three spontaneous regular menstrual cycles.
  • Severely anemic women (hemoglobin < 8gm/dl).
  • Women with any contraindications for POCs following the WHO eligibility (Altshuler AL et al., 2015).
  • Women refused to participate in the study.

研究组 & 干预措施

Group I "the depot medroxy-progesterone acetate group"

where they will use Depot Medroxyprogesterone Acetate 150 mg injection every 3 month,

干预措施: Depot medroxy-progesterone acetate (Drug)

Group II "Implanon group"

where they will have Implanon (etonogestrel implant) 68 mg implant

干预措施: Etonogestrel (Drug)

group III (cerazette group)

where they are using Cerazette pills (desogestrel 75 µg l) one pill every day for 28 days without pill-free interval.

干预措施: Desogestrel 75 µg (Drug)

结局指标

主要结局

Number of women developed vaginal bleeding

时间窗: 12 month

次要结局

未报告次要终点

研究者

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

Mohammed Khairy Ali

Lecturer

Assiut University

研究点 (1)

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