跳至主要内容
临床试验/2022-500922-13-00
2022-500922-13-00已完成3 期

Thiamine against chronic rheumatoid arthritis fatigue

Aarhus University Hospital1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2022年10月20日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
40
试验地点
1
主要终点
A change in fatigue level immediately after 4 weeks of high-dose thiamine treatment. The minimal clinically important difference (MCID) is a decrease of 7,43 points or an increase of 2,58 points on the BRAF-MDQ total fatigue score.

研究概览

简要总结

The main objective of this study is to investigate the efficacy of 4 weeks of high dose oral thiamine as treatment for chronic fatigue in patients with rheumatoid arthritis. The primary outcome is a change in fatigue level immediately after 4 weeks of treatment, measured using the Bristol Rheumatoid Arthritis Fatigue Multi-Dimensional Questionnaire (BRAF-MDQ).

入排标准

年龄范围
18 years 至 65+ years(18-64 Years, 65+ Years)
接受健康志愿者

入选标准

  • Rheumatoid arthritis diagnosed > 3 months ago.
  • In remission/mild disease activity (CRP < 10 mg/l, MD-HAQ < 1,3, DAS28 < 3,2)
  • Chronic fatigue (duration of fatigue ≥ 6 months, BRAF total fatigue score ≥ 16)
  • Age ≥18 years
  • Signed informed consent
  • Anticontraceptive (People who can get pregnant will need to use a safe anticontraceptive during the trial (12 weeks). Safe anticontraceptive is defined as: combination pills, intrauterine device, depot injection, subdermal implant, hormonal vaginal ring, or transdermal depot patch)

排除标准

  • Patients with co-morbidity which can explain the participants fatigue, including: Anaemia (haemoglobin < 7,1 mmol/l [female]; < 8,1 mmol/l [male], Iron deficiency (Ferritin < 30 μg/l), Vitamin B12 deficiency (Vitamin B12 <125 pmol/l), Folate deficiency (Folate < 9 nmol/l), Vitamin D deficiency (25-Hydroxy-Vitamin D[D3+D2] < 50 nmol/l), Diabetes (HbA1c ≥ 48 mmol/mol or medication), Hypo/hyperthyroidism (TSH <0,300 or > 4,5 IU/l or medication)
  • Participants who are unable to cooperate and follow the protocol
  • Pregnant patients

结局指标

主要结局

A change in fatigue level immediately after 4 weeks of high-dose thiamine treatment. The minimal clinically important difference (MCID) is a decrease of 7,43 points or an increase of 2,58 points on the BRAF-MDQ total fatigue score.

A change in fatigue level immediately after 4 weeks of high-dose thiamine treatment. The minimal clinically important difference (MCID) is a decrease of 7,43 points or an increase of 2,58 points on the BRAF-MDQ total fatigue score.

次要结局

  • A change in the patients’ quality of life at week 4, 8 and 12. Difference in EQ-5D score, MCID of 0,04.
  • A change in blood lactate concentration at week 4, 8 and 12.
  • Side effects to the treatment.

研究者

发起方
Aarhus University Hospital
申办方类型
Hospital/Clinic/Other health care facility
责任方
Principal Investigator
主要研究者

Department of Rheumatology, AUH

Scientific

Aarhus University Hospital

研究点 (1)

Loading locations...

相似试验