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临床试验/NCT00646802
NCT00646802已完成4 期

Vaginal Progesterone as a Maintenance Treatment in Women With Previous Preterm Labor. Randomized, Double Blinded, Placebo-controlled Trial

Hospital Clinic of Barcelona12 个研究点 分布在 1 个国家目标入组 265 人开始时间: 2008年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
265
试验地点
12
主要终点
Proportion of deliveries before week 34 of gestation

研究概览

简要总结

Eligible patients will be informed and asked to enroll in the study at hospital admission. A transvaginal ultrasound examination will be performed to determine cervical length. If an eligible woman accepts to participate, patient will be randomized to one of the study arms assigned in a double blind basis. Patient will receive the medication (vaginal capsule of progesterone or placebo). The patient will administer herself one vaginal capsule in a daily basis since gestational age of 36 weeks and 6 days as the primary endpoint is to demonstrate that the use of a maintenance treatment with vaginal progesterone is able to reduce the incidence of preterm birth before 34.0 and 37.0 gestational weeks. After delivery, perinatal and neonatal data will be collected.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Pregnant women aged between 18 - 45 years
  • Gestational age between 24.0 and before 33.6 gestational weeks
  • Singleton pregnancy
  • Patients admitted because of preterm labor who have been successfully treated of any tocolytic drugs (β-mimetics drugs, nifedipine, atosiban)
  • Ultrasound cervical length at discharge < 25 mm
  • Signed patient consent form (CI)

排除标准

  • Known or suspected infection, premature rupture of membranes or any other pathological gravid maternal or fetal condition coexisting at hospital admission (Pre-eclampsia, RCIU) which may induce iatrogenic labor.
  • Present or previous liver disease, present or previous cholestasis gravidarum, abnormal hepatic blood tests.
  • With known allergy to progesterone or peanuts (excipient).
  • Grade 2 (or upper) renal or liver laboratory abnormalities
  • Treated from dependent-hormone malignant cancer (i.e., breast carcinoma...)
  • With Diabetes mellitus or insulinized gestational diabetes
  • Treated with heparin
  • Drug abuse
  • Inadequate treatment compliance

研究组 & 干预措施

B

Placebo Comparator

Placebo

干预措施: Placebo (Drug)

A

Active Comparator

Progesterone 200 mg

干预措施: Progesterone (Drug)

结局指标

主要结局

Proportion of deliveries before week 34 of gestation

时间窗: week 34 of gestation

次要结局

  • Ultrasound cervical length(week +5)
  • Median time from randomization to delivery(delivery)

研究者

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

Montse Palacio

MD, PhD

Hospital Clinic of Barcelona

研究点 (12)

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