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临床试验/JPRN-UMIN000027270
JPRN-UMIN000027270招募中未知

A study on Prevention of Hypertensive Disorders of Pregnancy who have a history of severe hypertensive disorders of pregnancy -Pre-test for multi center trial

Mie university hospital, Department of Obstetrics and Gynecology0 个研究点目标入组 20 人开始时间: 2017年5月15日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
20

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
20years-old 至 ot applicable(—)
性别
Female

入选标准

  • 1) 20 years of age or older
  • 2) History of severe Hypertensive disorders of Pregnancy that required delivery prior to 34 weeks' gestation.
  • 3) Gestational age between 12 + 0 and 16 + 6 weeks (The expected date of confinement is determined using the criteria of the guidelines for obstetrical practice in Japan 2014.)
  • 4) Singleton pregnancy
  • 5) For the test participation, it has consent is obtained in writing from the patient.

排除标准

  • 1)A history of allergy to tadalafil
  • 2)Concurrent medications that interact adversely with tadalafil
  • 3)Relative contraindication of tadalafil treatment due to renal disease.
  • 4)Relative contraindication of tadalafil treatment due to liver disease.
  • 5)Relative contraindication of tadalafil treatment due to uncontrolled arrhythmia, hypertension (BP >170/110 mmHg), and hypotension (BP <80/40 mmHg).
  • 6)Fetus with suspected chromosomal disorder and/or multiple congenital anomalies.
  • 7)Relative contraindication of tadalafil treatment due to retinitis pigmentosa, coagulation defect, active gastric and/or intestinal ulcer, and venous obstructive disease.
  • 8)Attending physician decides to entry inappropriate.

研究者

发起方
Mie university hospital, Department of Obstetrics and Gynecology

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