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临床试验/NCT01119963
NCT01119963已完成2 期

17-alpha-Hydroxyprogesterone Caproate (17P, Makena®) for Prolongation of Pregnancy in Women With Preterm Rupture of the Membranes (PROM), Double-blinded Randomized Clinical Trial

Obstetrix Medical Group14 个研究点 分布在 1 个国家目标入组 152 人开始时间: 2011年10月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
152
试验地点
14
主要终点
Gestational Age at Delivery

研究概览

简要总结

The objective of the study is to determine if a weekly dose of 17 hydroxyprogesterone caproate (17P, Makena®) given to women with preterm rupture of the membranes will:

  1. increase the probability of continuing the pregnancy until a favorable gestational age.
  2. increase the interval between randomization and delivery.
  3. decrease neonatal morbidity.

详细描述

Preterm rupture of the membranes (PROM) is the leading identifiable cause of prematurity and accounts for about one-third of all preterm deliveries and 18-20% of perinatal deaths in the USA. When PROM occurs at very early gestational ages, the clinician must make a decision whether to attempt to prolong the pregnancy or whether to recommend prompt delivery. Both approaches carry substantial risk. The strategy of continuing the pregnancy is commonly called "expectant management." During expectant management, gestational age steadily increases, and the balance naturally shifts toward favoring delivery. Once the gestational age reaches 34 weeks, the risk of lethal or permanent sequelae of prematurity or minimal, so most clinicians agree that delivery is warranted. Despite an attempt at expectant management, the majority of patients with PROM will be delivered within the first week or so. Unfortunately, no intervention other than antibiotic prophylaxis or corticosteroids have been shown to prolong latency or reduce neonatal morbidity after PROM. Recent evidence suggests that prophylactic administration of progesterone medications may reduce the risk of preterm delivery in women with certain risk factors, notably those with a history of a prior preterm delivery and those with a shortened cervix discovered by ultrasound examination. Clearly, women with PROM are at very high risk of preterm delivery, so there is a pressing need to study whether 17 hydroxyprogesterone caproate (17P) is effective after PROM. Progesterone might be beneficial after PROM both because it tends to promote uterine quiescence by suppressing the formation of myometrial gap junctions and because it has anti-inflammatory properties, suppressing the production of inflammatory cytokines and thereby inhibiting cervical ripening. Inflammation is a major pathway leading to preterm labor, cervical dilation & preterm delivery. 17P would seem to be like an ideal candidate for prolongation of pregnancy after PROM.

This is a double-blinded, placebo-controlled, multicenter, randomized clinical trial of 17P versus placebo. The primary outcome measure will be the percentage of each group reaching either a gestational age of 34w0d or documentation of fetal lung maturity at 32w0d to 33w6d. Secondary outcomes will include the latency period for each group and the percentage of newborns in each group who have major neonatal morbidity or death.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Participant is 18 years old or older
  • Gestational Age (GA) 23w0d and 30w6d @ time of enrollment
  • Singleton pregnancy
  • PROM defined as either (a) or (b) or (c) below (a) Documentation of vaginal leakage of indigo carmine dye instilled via amniocentesis (b) Positive Amnisure® test (c) Two or more of (i) through (iv): i. Nitrazine test with pH of 7 or more ii. Positive fern test iii. Gross pooling of clear fluid iv. US exam showing oligohydramnios

排除标准

  • Any contraindication to expectant management
  • Any fetal condition likely to cause serious neonatal morbidity independent of gestational age
  • History of allergy to 17P
  • Any contraindications to 17P use (e.g. Thrombosis, Breast CA, abnormal vaginal bleeding unrelated to pregnancy, jaundice, liver disease, uncontrolled HTN)
  • Any medical condition currently treated with systemic steroid medications
  • Cervical cerclage present at the time of PROM
  • Informed consent not obtained.

研究组 & 干预措施

17-alpha hydroxyprogesterone caproate, Makena®

Active Comparator

250 mg of 17P, Makena® intramuscular (IM) weekly.

干预措施: 17-alpha-hydroxy-progesterone caproate, Makena® (Drug)

Placebo

Placebo Comparator

Castor Oil (Placebo)intramuscular (IM) weekly

干预措施: Castor Oil (Placebo) (Drug)

结局指标

主要结局

Gestational Age at Delivery

时间窗: Measured from day of last menstrual cycle to day of birth and measured in weeks.

Gestational age is measured in weeks, from the first day of the woman's last menstrual cycle to the date the baby was born.

次要结局

  • Duration of Latency Period(average number of days measured from day of study entry until day of delivery)

研究者

发起方
Obstetrix Medical Group
申办方类型
Industry
责任方
Sponsor

研究点 (14)

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