EUCTR2016-004112-35-SE进行中(未招募)1 期
ow-dose azathioprine and allopurinol- versus azathioprine monotherapy in patients with Inflammatory Bowel Disease: An investigator-initiated, open, multicentre, parallel-arm, randomized controlled trial A SOIBD (The Swedish Organisation for the study of Inflammatory Bowel Diseases) study
SOIBD (The Swedish Organisation for the study of Inflammatory Bowel Diseases)0 个研究点目标入组 120 人开始时间: 2017年6月21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
- 入组人数
- 120
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
- All
入选标准
- •1.Age 18-80 years at the time of inclusion, weight between 50 and 100 kg.
- •2.Willingness to comply with all trial procedures and being available for the duration of the trial.
- •3.Clinical and histological verified IBD eligible for treatment with thiopurines due to steroid dependence (failure to taper steroid or starting a second course of systemic steroids within one year) or due to the need for thiopurines for other reasons (disease phenotype, i.e post-surgery decision).
- •4.A written informed consent to participate in the study is signed before any study-related procedures are performed.
- •5.A normal TPMT activity measurement (>8.9 U/ml RBC) or normal TPMT genotype (*1/*1).
- •6.Naïve to thiopurine treatment
- •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 100
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 20
排除标准
- •1.Biologic treatment (anti-TNF, vedoluzimab etc) within the last three months prior the study
- •2.Concurrent participation in another interventional therapy study.
- •3.Females who are pregnant or breastfeeding
- •4.Females of childbearing age and potential who are not willing or capable to use acceptable methods of contraception (oral contraceptives, condoms, diaphragms, intrauterine devices) during the entire study and for up to 3 months after the end-of-study evaluation.
- •5.Male patients who do not use acceptable barrier methods of contraception (condoms) during the entire course of the study and up to 3 months after the end-of-study evaluation.
- •6.Inability to follow the treatment protocol (as judged by the investigator)
- •7.Current treatment with Allopurinol.
- •8.Patients with gout that needs medical treatment.
- •9.Estimated GFR < 50 ml/ml
- •10.Persistent alanine aminotransferase U/L (ALT) above upper limit of the normal range.
研究者
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