跳至主要内容
临床试验/NCT05139498
NCT05139498进行中(未招募)不适用

Conservative Management as an Alternative to Hysterectomy for Placenta Accreta Spectrum: a Pilot Randomized Controlled Trial.

University of Utah1 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2022年5月26日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
4
试验地点
1
主要终点
Number of patients completing the surgical treatment to which they are allocated

研究概览

简要总结

Conservative in situ management is a promising alternative treatment to hysterectomy for patients with placenta accreta spectrum and may be safer and preferable for some patients. This study will assess feasibility of a future randomized clinical trial comparing these treatments and provide novel data to inform shared decision-making and cost-effective care for patients with this deadly pregnancy disorder.

详细描述

Placenta accreta spectrum (PAS) is an extremely morbid and increasingly common pregnancy condition that often results in massive obstetric hemorrhage. The standard treatment in the United States is hysterectomy, but this treatment is complex, morbid, and costly. A promising alternative for PAS treatment is conservative in situ management (CM), a strategy in which the placenta is left in the uterus. Unfortunately, there are insufficient data available to compare outcomes of these two treatments because past studies are limited by non-randomized study designs, minimal inclusion of patient values in making treatment decisions, and nominal consideration of economic barriers to care. A large clinical trial comparing PAS treatments is needed. But there are key logistic barriers to an adequately powered trial, including questions of whether patients will enroll and adhere to randomization allocation. This pilot trial will evaluate the feasibility of randomizing patients to CM versus hysterectomy for PAS.

While pilot studies cannot make final assessments of safety and efficacy between interventions, safety and efficacy will be monitored, including those related to hemorrhage, transfusion, infection and re-operation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
Female
接受健康志愿者
否

入选标准

  • •Age 18 and older
  • •History of cesarean delivery AND placenta previa OR anterior low-lying placenta AND suspected of having PAS on prenatal imaging (ultrasound/MRI)
  • •Patients who would typically be recommended for hysterectomy
  • •Planned delivery between 34w0d and 36w0d gestation.

排除标准

  • •Plan to delivery before neonatal viability (<24 weeks gestation)
  • •Hospitalized for antenatal hemorrhage
  • •Have a low antenatal suspicion for PAS based on imaging
  • •Are pregnant with multiples (twins, triplets)
  • •Have a uterine fetal demise

研究组 & 干预措施

Conservative Management for Placenta Accreta Spectrum (PAS)

Experimental

Subjects who are randomized to to conservative management will undergo a cesarean delivery followed by a period of close observation in the operating room for 30-45 minutes to be sure there is no excessive bleeding or risk to keep the placenta inside

干预措施: Conservative management for placenta accreta spectrum (PAS) (Procedure)

Hysterectomy at time of delivery for Placenta Accreta Spectrum (PAS)

Active Comparator

Subjects who are randomized to cesarean hysterectomy will undergo a cesarean delivery followed immediately by hysterectomy to remove the placenta and uterus together

干预措施: Cesarean hysterectomy for placenta accreta spectrum (PAS) (Procedure)

结局指标

主要结局

Number of patients completing the surgical treatment to which they are allocated

时间窗: Day of delivery

Number of patients completing the surgical treatment to which they are allocated (hysterectomy or conservative management) on the day of delivery.

次要结局

  • Number of eligible people approached for enrollment.(20 weeks gestation through day of delivery)
  • Number of enrolled completing hysterectomy on day of delivery.(Day of delivery)
  • Number of enrolled completing conservative management on day of delivery.(Day of delivery)
  • Number of eligible people randomized.(From time of consent up to one week (1-7 days) before planned delivery)
  • Number of enrolled who are lost to follow-up through study end (inverse of retention).(Up to 6 weeks postpartum)
  • Number of enrolled who don't complete their allocated treatment (drop-out).(Up to 6 weeks postpartum)
  • Number of enrolled completing full postpartum follow-up visit schedule.(Up to 6 weeks postpartum)

研究者

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

Brett Einerson

Principal Investigator

University of Utah

研究点 (1)

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