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临床试验/CTIS2024-512453-25-00
CTIS2024-512453-25-00进行中(未招募)1 期

Efficacy, tolerability and preferences of per oral or subcutaneous methotrexate in patients with early rheumatoid arthritis – a randomised register based multicentre study - MTXRA

Region Vaesterbotten0 个研究点目标入组 212 人开始时间: 2024年6月3日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
212

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
18 至 65+(—)
性别
All

入选标准

  • The subject has given written consent to participate in the study, Diagnosis of rheumatoid arthritis by rheumatologist fulfilling 2010 Rheumatoid Arthritis Classification Criteria, Indication of methotrexate, 18-95 years of age, Women of Childbearing Capacity (WOCBC) must: a) Comply to use of highly effective contraception methods during the course of the trial. b) Have a negative pregnancy test., Male patients included in the study that have fertile female partners must use adequate contraception within their relationship during the same period of time

排除标准

  • Contraindications for methotrexate, Previous treatment with any DMARD within the last five years, Known or suspected allergies against methotrexate or any other substance in the given medication, Anamnestic information on pregnancy, breastfeeding, or planned pregnancy, Mental inability, reluctance or language difficulties that result in difficulty understanding the meaning of study participation or inability to answer questionnaire in written Swedish, Treatment or disease which, according to the investigator, can affect treatment or study results., Fear of needles leading to not being able to use subcutaneous injections, For the study in gut microbiota: Use of antibiotics or probiotics within the last 3 months

研究者

发起方
Region Vaesterbotten

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