跳至主要内容
临床试验/EUCTR2007-003706-10-FI
EUCTR2007-003706-10-FI进行中(未招募)不适用

Satunnaistettu, etenevä tutkimus keskeytyslääkkeiden annostelusta toisen raskauskolmanneksen aikaisissa keskeytyksissä

Maarit Mentula0 个研究点目标入组 200 人开始时间: 2007年10月19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
入组人数
200

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

  • 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)
  • F.1.3.1 Number of subjects for this age range

排除标准

  • 未提供

研究者

发起方
Maarit Mentula

相似试验

尚未招募
不适用
A clinical Trial of Mukhakantiprada lepa and its cream on human patients of hyperpigmentation on face
CTRI/2019/05/019385Sane guruji Arogya kendra
进行中(未招募)
不适用
Estudio aleatorizado de interrrupción de tratamiento con NatalizumabRandomized Treatment Interruption of Natalizumab - RESTOREEl natalizumab es un medicamento muy eficaz utilizado en el tratamiento de pacientes con esclerosis múltiple (EM) recidivante.Se trata de un estudio prospectivo y aleatorizado, en pacientes con formas recidivantes de la EM que han recibido tratamiento con natalizumab durante un mínimo de 12 meses, sin recaídas durante ese tiempo.MedDRA version: 11Level: LLTClassification code 10063399Term: Esclerosis múltiple remitente-recurrente
EUCTR2009-017490-38-ESBiogen Idec Ltd200
进行中(未招募)
不适用
Clinical study to assess the pharmacokinetics, safety & tolerability of single and multiple oral doses of AFQ056 in children with Fragile X Syndrome
EUCTR2011-004867-65-Outside-EU/EEAovartis Pharma Services AG24
进行中(未招募)
1 期
Clinical study to assess the pharmacokinetics, safety & tolerability of single and multiple oral doses of AFQ056 in children with Fragile X Syndrome
EUCTR2011-004867-65-ESovartis Farmacéutica, S.A.21
进行中(未招募)
1 期
Pharmacoepidemiology study to define the long-term safety profile of tenofovir disoproxil fumarate (Tenofovir DF, Viread®) and describe the management of Tenofovir DF-associated renal and bone toxicity in Chronic Hepatitis B (CHB)-infected adolescents aged 12 to <18 years in EuropeChronic Hepatitis BMedDRA version: 20.1Level: PTClassification code 10008910Term: Chronic hepatitis BSystem Organ Class: 10021881 - Infections and infestations
EUCTR2014-004939-39-FRGilead Sciences International Ltd.100