NL-OMON49995招募中不适用
A Pilot-study to determine the (cost) effectiveness of the adhesion barrier 4DryField® PH in prevention of dysmenorrhea, abdominaal pain and niche-related problems after caesarean sections - 4DryField Study
适应症
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 114
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
- •- Patients who underwent their first CS (primary or secondary)
- •- Sufficient command of the Dutch or English language
- •- >= 18 years old
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
研究者
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