NL-OMON48848招募中不适用
Mental wellbeing and quality of life after insertion of a LNG-IUD or Cu-IUD. A randomized patient preference trial. - Quality of life after LNG-IUD versus Cu-IUD (E-CHIQ study).
oordwest Ziekenhuisgroep0 个研究点目标入组 394 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 入组人数
- 394
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
- 年龄范围
- 18 至 99（—）
入选标准
- •- Age; between 18 and 45 years.
- •- Wish for LARC by means of a LNG-IUD or Cu-IUD for a minimum period of 12 months.
- •- Willing to fill out 5 questionnaires, taking 15 to 20 minutes per questionnaire.
- •- Access to internet and sufficient understanding of Dutch language.
- •- Willing to provide informed consent.
排除标准
- •Cu-IUD insertion as emergency contraception.
- •Patients with heavy bleeding pattern/problems or with a wish for less blood-loss.
- •Patients with an Cu-IUD or LNG-IUD < 3 months prior to placement this IUD
- •IUD insertion while being under general anaesthetics.
- •IUD insertion within 6 weeks postpartum and 12 weeks after a caesarean are excluded.
- •Contraindications according to the product leaflets.
- •patients taking medication against a mental conditions
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