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Fatigue and Skeletal Muscle Impact in Severe Axial Spondylarthritis (Famuspa)

2019年5月10日 更新者:University Hospital, Strasbourg, France

Axial spondyloarthropathy (SpA) is the most common inflammatory rheumatism (1% of the general population) with important medico-economic consequences.

Fatigue is a major feature of SA. It can be defined as a feeling of reduced muscle capacity, lack of energy and exhaustion. The fatigue reaches an abnormally high level (fatigue severity score (FSS) ≥4, called severe fatigue in this protocol) in more than two thirds of patients with SA.

Skeletal muscle repercussions are present during SA. It is characterized by a decrease in exercise capacity independently of pain and ankylosis but is associated with a decrease in strength and muscle mass, the importance of which varies from one study to another.

The link between fatigue (subjective sensation) and the skeletal muscular impact (objective) of SA has never been studied.

研究概览

详细说明

This work will:

  1. • To study for the first time the implication of the objective skeletal muscular impact in fatigue during SA.
  2. • To better characterize the skeletal muscle impact of SA;
  3. • To characterize the evolution of the fatigue and the muscular impact under anti-TNFα treatment and the predictive factors of response,
  4. • To identify new therapeutic targets for these two complications of SA, which currently have no specific treatment.

研究类型

介入性

注册 (预期的)

125

阶段

  • 不适用

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 及以上 (成人、年长者)

接受健康志愿者

有资格学习的性别

全部

描述

Inclusion criteria:

-- Axial SA according to the ASAS criteria;

  • Indication to start a biotherapy;
  • ≥ 18 years old, no upper age limit;
  • Subject affiliated to a social health insurance reimbursement;
  • Subject having signed a dated and informed consent;
  • Woman in childbearing age: negative beta-HCG test and effective contraception;
  • Sufficient understanding of French to follow the protocol.

Exclusion criteria:

  • Biologic treatments (ongoing or or taken during the 6 months preceding the study),
  • Associated extramuscular inflammatory disease (s) (excluding ocular and cutaneous involvement) eg chronic inflammatory bowel disease
  • Contraindication to the use of a biologic
  • Associated fibromyalgia (Questionnaire score FiRST ≥5) achieved during the V0 visit
  • History of coronary artery disease: exercise angina, acute coronary syndrome and / or coronary angioplasty,
  • History of lower extremity arterial disease: vascular claudication and / or lower extremity angioplasty
  • COPD
  • Neuromuscular pathology
  • Insufficiency of organ (renal, hepatic pulmonary heart)
  • Sleep apnea
  • Impossibility of giving the subject informed information (subject in emergency situation, difficulties in understanding the subject, etc.)
  • Subject under the protection of justice
  • Subject under guardianship or curatorship
  • Breastfeeding
  • Pregnancy
  • Subject in exclusion period defined by another clinical study or participating in a study likely to impact the results of the research
  • Corticosteroids in the 15

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:非随机化
  • 介入模型:并行分配
  • 屏蔽:无(打开标签)

武器和干预

参与者组/臂
干预/治疗
其他:anti-TNFα treatment and severe fatigue (FSS)

See bellow (section "Interventions") the full description for

  • Measurement of aerobic exercise on cycloergometer
  • Measurement of muscle mass by two-photon absorptiometry: specific study
  • Measurement of Isometric Muscle Strength
  • Blood sampling for measurement of cytokine levels in the blood
  • Measurement of sedentarity
  • Psychological impact
  • Fatigue mesurement
  • Needle muscle of the vastus lateralis (This act will be limited to patients in care at Strasbourg University Hospital n=30)

The incremental effects tests will be performed in a service specialized in the exploration of the exercise (physiology or cardiology according to the centers) in a spacious and air-conditioned room, in the presence of a medical specialist. exercise and close to the resuscitation equipment.

Before the test, weight and height will be collected. Information on the conduct of the test will be given to the patient. A multi-derivation ECG recording will be detected throughout the duration of the test and followed by a physician experienced in the ECG effort.

O2 saturation by oximetry of hens will be recorded continuously. Blood pressure will be recorded at each level. The collection of expired gases in the face mask whose tightness will be verified to measure the fractions inspired and expired in O2 and CO2 (Sensor Medics Vmax229, Yorba Linda, CA, USA) and calculations VO2 max and VCO2.

Maximal power (W max) will be recorded Patients will be encouraged during the test.

其他:anti-TNFα treatment and with mild fatigue (FSS <4)

See bellow (section "Interventions") the full description for

  • Measurement of aerobic exercise on cycloergometer
  • Measurement of muscle mass by two-photon absorptiometry: specific study
  • Measurement of Isometric Muscle Strength
  • Blood sampling for measurement of cytokine levels in the blood
  • Measurement of sedentarity
  • Psychological impact
  • Fatigue measurement
  • Needle muscle of the vastus lateralis (This act will be limited to patients in care at Strasbourg University Hospital n=30)

The incremental effects tests will be performed in a service specialized in the exploration of the exercise (physiology or cardiology according to the centers) in a spacious and air-conditioned room, in the presence of a medical specialist. exercise and close to the resuscitation equipment.

Before the test, weight and height will be collected. Information on the conduct of the test will be given to the patient. A multi-derivation ECG recording will be detected throughout the duration of the test and followed by a physician experienced in the ECG effort.

O2 saturation by oximetry of hens will be recorded continuously. Blood pressure will be recorded at each level. The collection of expired gases in the face mask whose tightness will be verified to measure the fractions inspired and expired in O2 and CO2 (Sensor Medics Vmax229, Yorba Linda, CA, USA) and calculations VO2 max and VCO2.

Maximal power (W max) will be recorded Patients will be encouraged during the test.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Oxygen consumption capacity
大体时间:At inclusion
Maximum oxygen consumption capacity on cycloergometer during an incremental effort until exhaustion (VO2 max)
At inclusion

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (预期的)

2019年9月12日

初级完成 (预期的)

2019年12月12日

研究完成 (预期的)

2022年9月12日

研究注册日期

首次提交

2019年5月6日

首先提交符合 QC 标准的

2019年5月6日

首次发布 (实际的)

2019年5月7日

研究记录更新

最后更新发布 (实际的)

2019年5月13日

上次提交的符合 QC 标准的更新

2019年5月10日

最后验证

2019年5月1日

更多信息

与本研究相关的术语

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研究美国 FDA 监管的设备产品

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