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临床试验/EUCTR2018-004179-11-NL
EUCTR2018-004179-11-NL进行中(未招募)1 期

Effectiveness of Somatostatin Analogues in Patients with hereditary hemorrhagic telangiectasia and symptomatic gastrointestinal bleeding, the SAIPAN-trial: a multicenter, randomized, open-label, parallelgroup, superiority trial. - SAIPAN-trial

Radboudumc0 个研究点目标入组 38 人开始时间: 2019年5月14日最近更新:
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
Radboudumc
入组人数
38

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

入选标准

  • - Patients older than 18 years with written informed consent.
  • - Diagnosis of HHT: either confirmed by genetic testing or the Curacao criteria (definite
  • diagnosis).
  • - Presence of IDA in combination with the presence endoscopic proven GI AVM manifestations /
  • telangiectasias confirmed within the last 12 months (upper and/or lower endoscopy and/or
  • capsule endoscopy).
  • - Endoscopic refractory: at least 1 endoscopic APC / laser /other endoscopic treatment modality
  • performed in the past 5 years.
  • - Substantial transfusion dependency: at least 4 blood units and / or intravenous iron in the 6
  • months prior to study inclusion with a:
  • o At least one serum ferritin below < 30 ug/l within the last 6 months requiring iron
  • infusion above or equal to 1 g and/or
  • o Hemoglobin below 5.6 mmol/l (9.0 g/dl) or are in need of transfusions due to anemia related symptoms within the last 6 months requiring blood transfusion above.
  • 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 30
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 8

排除标准

  • - liver cirrhosis child-pugh C.
  • - symptomatic cholecystolithiasis (possible side-effect octreotide).
  • - pregnancy or nursing women or women have a pregnancy wish during the study period.

研究者

发起方
Radboudumc

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