NL-OMON23062尚未招募不适用
A Pilot-study to determine the (cost)effectiveness of the adhesion barrier 4DryField® PH in prevention of dysmenorrhea, pain and niche-related problems after Caesarean sections
Amsterdam UMC, VUmc0 个研究点目标入组 110 人开始时间: 待定最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 110
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
入选标准
- •Patients undergoing their first CS (planned or unplanned)
- •-Age = 18 years
排除标准
- •-Patients with an indication for an emergency CS (suspicion of fetal distress), or patients in heavy pain without accurate therapy, and who were not informed about this study during pregnancy
- •-Previous uterine major surgery (e.g. laparoscopic or fibroid resection by laparotomy, septum resection)
- •-Patients with known causes of menstrual disorders (known cervical dysplasia, communicating hydrosalpinx, uterine anomaly or endocrine disorders disturbing ovulation) or use of medication that can influence the frequency of blood loss (e.g. Ascal).
- •-Placenta percreta during the current pregnancy
- •-Patients with chronic abdominal pain
- •-Patients who do not speak Dutch or English
研究者
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