Comparison of Tripterygium wilfordii Hook F with methotrexate in the treatment of active rheumatoid arthritis (TRIFRA): a randomised, controlled clinical trial

التفاصيل البيبلوغرافية
العنوان: Comparison of Tripterygium wilfordii Hook F with methotrexate in the treatment of active rheumatoid arthritis (TRIFRA): a randomised, controlled clinical trial
المؤلفون: Qun Shi, Qian-wen Lv, Wan-lan Jiang, Bin Liu, Ying Jiang, Xin Li, Fu-lin Tang, Wenjie Zheng, Lu Gong, Hongtao Jin, Lidan Zhao, Wei Wei, Jun-xiang Wang, Hua Chen, Jing-mei Su, Ai-jing Liu, Wen Zhang, Xuan Zhang, Hui Liu, Yunyun Fei, Min Shen, Qian Wang, Di Liang, Peter E. Lipsky, Xiangni Wu, Qingjun Wu, Yufeng Yin, Hongbin Li, Xiumei Liu, Zhen-bin Li, Jing Li, Fengchun Zhang
المصدر: Europe PubMed Central
مصطلحات موضوعية: Adult, Male, musculoskeletal diseases, medicine.medical_specialty, Tripterygium, Immunology, Arthritis, Gastroenterology, General Biochemistry, Genetics and Molecular Biology, law.invention, Arthritis, Rheumatoid, Rheumatology, Randomized controlled trial, law, Internal medicine, medicine, Humans, Immunology and Allergy, Single-Blind Method, biology, Plant Extracts, business.industry, Middle Aged, biology.organism_classification, medicine.disease, Surgery, Clinical trial, Irregular menstruation, Methotrexate, Treatment Outcome, Antirheumatic Agents, Rheumatoid arthritis, Female, Tripterygium wilfordii, medicine.symptom, business, Phytotherapy, medicine.drug
الوصف: ObjectivesTo compare the efficacy and safety of Tripterygium wilfordii Hook F (TwHF) with methotrexate (MTX) in the treatment of active rheumatoid arthritis (RA).MethodsDesign: a multicentre, open-label, randomised controlled trial. All patients were assessed by trained investigators who were unaware of the therapeutic regimen. Intervention: 207 patients with active RA were randomly allocated (1:1:1) to treatment with MTX 12.5 mg once a week, or TwHF 20 mg three times a day, or the two in combination. At week 12, if reduction of the 28-joint count Disease Activity Score (DAS28) was Results174/207 (84.1%) patients completed 24 weeks of the trial. In an intention-to-treat analysis, the proportion of patients reaching the ACR50 response criteria was 46.4% (32/69), 55.1% (38/69) and 76.8% (53/69), respectively, in the MTX, TwHF and MTX+TwHF groups (TwHF vs MTX monotherapy, p=0.014; MTX+TwHF vs MTX monotherapy, p0.05). The result of per-protocol analysis agreed with that seen in the intention-to-treat analysis. Seven, three and five women in the TwHF, MTX and combination groups, respectively, developed irregular menstruation (TwHF vs MTX monotherapy, p=0.216).ConclusionsTwHF monotherapy was not inferior to, and MTX+TwHF was better than, MTX monotherapy in controlling disease activity in patients with active RA.Trial registration numberNCT01613079.
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab81a7688ba70e6371f4579b2a8658a2
http://europepmc.org/abstract/med/24733191
رقم الأكسشن: edsair.doi.dedup.....ab81a7688ba70e6371f4579b2a8658a2
قاعدة البيانات: OpenAIRE