跳至主要内容
临床试验/EUCTR2009-014302-34-IT
EUCTR2009-014302-34-IT进行中(未招募)不适用

Prophylaxis of hypotension in Caesarean Section: comparison between plasma expander hydroxyethyl starch and isotonic polyelectrolytic balanced solution. - OST-01-2009

AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI0 个研究点开始时间: 2010年5月7日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
发起方

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • Acquisition of Informed Consent;
  • ? ASA 1-2;
  • ? aged between 18 and 40 years,
  • ? height of between 150-170 cm,
  • ? body weight between 50 and 90 kg,
  • ? undergoing caesarean in election or in planned emergency.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • ? obstetric pathologies with hemorrhagic risk (central placenta ..)
  • ? twin pregnancies and plurigemine,
  • ? congenital or acquired abnormalities of coagulation,
  • ? permagna obesity,
  • ? skin infections or previous or current diseases of the spine,
  • ? patients with ASA> 2,
  • ? Patients undergoing urgent cesarean section
  • ? serious medical conditions that, in the opinion of the investigator, contraindicated inclusion of patient participation in the study;
  • ? use of experimental drugs in the last two months before inclusion in the study.
  • ? Patients unable to follow the procedures laid down by the Protocol and to sign informed consent. In the case of patients unable to give informed consent to the study, the procedure must be provided and signed by guardian or legal representative. Patients, that are unable to sign the consent, must sign as they are able to do so.

研究者

发起方
AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI

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