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临床试验/NCT03930407
NCT03930407Unknown不适用

Serum Antimullerian Hormone Levels in Patients Who Underwent Hayman Suture for Uterine Atony During Cesarean Section

Kanuni Sultan Suleyman Training and Research Hospital1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2019年4月15日最近更新:
适应症

试验速览

阶段
不适用
入组人数
120
试验地点
1
主要终点
Change in follicle stimulating hormone level from baseline (precesarean) to post-cesarean

研究概览

简要总结

From patient charts we will review patients who had undergone cesarean section within the last 6 months and identify those who received a The Hayman uterine compression suture for uterine atony. We will also select patients who delivered a baby without recieving a Hayman suture to create a control group. Patietns will be grouped as Hayman Group if they recevied a Hayman suture during C/S and control group if thay had not recevied a Hayman suture. We will then check patient charts for post-cesarean outpatient clinic visit and select those who received ovarian reserve evaluation via hormones and antral follicle count during the visits. Finally, we are planning to investigate any correlation between Hayman suture and ovarian dysfunction.

详细描述

Hayman suture is a common technique for uterine compression to stop bleeding due to uterine atony. Hayman described placement of two to four vertical compression sutures from the anterior to posterior uterine wall without hysterectomy. It is usually employed to overcome uterine atoy dıring cesarean section. However, since the technique is relatively new, data on its safety and efficacy arelimited to a few case reports. several complications including cavity obliteration, blood entrapment and infections have been described. However, data regarding the ovarioan function is lacking.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Retrospective

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

  • age 18- 40 years
  • no systemic or endocrine diseases
  • patients who had uterine artery ligation due to atony
  • healthy postpartum patients as controls

排除标准

  • patients with Polyctsitic over syndrome
  • Pregnancy with IVF or oocyte donation
  • Obese patients
  • patients with previous/present endometriosis

结局指标

主要结局

Change in follicle stimulating hormone level from baseline (precesarean) to post-cesarean

时间窗: Before cesarean section and at any follow-up visit within 6 months of cesarean section

IU/L

Change in luteinizing hormone level from baseline (precesarean) to post-cesarean

时间窗: Before cesarean section and at any follow-up visit within 6 months of cesarean section

mU/mL

Change in anti-mullerian hormone level from baseline (precesarean) to post-cesarean

时间窗: Before cesarean section and at any follow-up visit within 6 months of cesarean section

ng/dl

次要结局

  • Antral follicle count in the two study groups(At any follow-up visit within 6 months of cesarean section)

研究者

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

Aysu Akca

Principal Investigator

Kanuni Sultan Suleyman Training and Research Hospital

研究点 (1)

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