跳至主要内容
临床试验/NCT05416697
NCT05416697已完成3 期

Effectiveness of Cannabinoid on Appetite, Sleep Quality, Quality of Life, Joint Pain, and Cytokine Level in Systemic Sclerosis Patients: a Randomized Placebo-controlled Trial

Khon Kaen University2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年11月9日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
入组人数
30
试验地点
2
主要终点
The changing of appetite

研究概览

简要总结

The cannabinoid has benefits in many aspects but the evidence of the effect of cannabinoids in humans with SSc is limited. We, therefore, would like to investigate the efficacy of cannabinoids on the appetite, sleep efficiency, quality of life, pain, and critical cytokine level in SSc compared with placebo in SSc patients and the adverse events associated with cannabinoids in those patients.

详细描述

Systemic sclerosis (SSc) is a connective tissue disease for which skin tightness is the hallmark. The disease is classified into 2 major subsets: limited cutaneous systemic sclerosis (lcSSc) and diffuse cutaneous systemic sclerosis (dcSSc) depending on the extent of skin tightness. Not only the skin tightness but also the internal organs such as the musculoskeletal, kidneys, lungs, heart, and intestines can be involved and associated with a poor outcome. Malnutrition and/or weight loss is a complications in SSc. The complication is possibly related to gastrointestinal involvement, inflammation, immunosuppressant agents, or mood disturbance which can affect the food appetite or eating behavior. As well as sleep quality, sleep disturbance has been reported in SSc patients and the associated factor of sleep disturbance in those patients was gastrointestinal involvement, particularly gastroesophageal reflux disease, the severity of pain, and depressed mood. The cannabinoid is an agent which affects appetite, pain, and sleep quality as mentioned above, hence it would improve the appetite, get a high sleep quality and reduce pain associated with musculoskeletal involvement in SSc patients.

Although cannabinoid has benefit in many aspects, they also resulted in serious adverse events after cannabinoid inhalation, including ischemic stroke related to vasospasm of the cerebral vessel, high cardiac output, cardiac arrhythmias, blood pressure fluctuation, and respiratory tract infection. Acute toxicity has been reported and depended on unit dose, tolerance, and route of cannabinoid use. Cannabis also influenced brain function including memory, and cognitive function, and expanded the risk for psychosis in those who had prolonged use. The symptoms of central nervous system (CNS) toxicity include euphoria, panic, agitation, mood alterations, alteration of perception, loss of social inhibition, muscle incoordination, myoclonic jerking, ataxia, slurred speech, and risk of the suicidal idea. In addition, prolonged high doses of cannabis use can lead to the development of cannabinoid hyperemesis syndrome caused by cyclic hyperemesis, finally resulting in electrolyte disturbances and impaired kidney function.

Because the evidence of the effect of cannabinoids in humans with SSc is limited. We, therefore, would like to investigate the efficacy of cannabinoids on the appetite, sleep efficiency, quality of life, pain, and key cytokine level in SSc compared with placebo in SScpatientst and the adverse events associated with cannabinoids in those patients.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Outcomes Assessor)

盲法说明

The participant, care provider, and assessor will be blinded.

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •SSc patients aged between 18 and 70 years
  • •Diagnosed according to ACR/EULAR 2013 classification criteria
  • •Having anorexia or malnutrition status
  • •Must not receive steroid equivalent to prednisolone dose more than 10 mg/d
  • •Must receive a stable dose of steroid, immunosuppressant, and/or vitamin or its supplement within 2 weeks before enrollment
  • •Must stop anxiolytics, hypnotics, or sleeping pills at least 2 weeks before enrollment
  • •Understand and able to read and write the Thai language

排除标准

  • •Overlap with other connective tissue diseases
  • •Pregnancy or lactation
  • •Bedridden and confined to no self-care
  • •Evidence of active malignant disease
  • •Present uncontrolled or severe medical problems including diabetes mellitus, asthma, angina, cardiovascular, thyroid, hepatic, or renal diseases (Cr>1.4 mg/dl)
  • •Present active infection that needs systemic antibiotic
  • •Previous allergy to cannabinoid or their derivatives
  • •Concomitant illegal drug used (amphetamine or its derivative, cocaine)
  • •History of the previous cannabinoid using or concomitant any herbal included cannabinoid used
  • •On-going anxiolytics, hypnotics, or sleeping pills used
  • •In a period that needs immunosuppressant dose adjustment
  • •Having active SSc that needs closed monitoring for disease progression (pulmonary hypertension, proteinuria, microscopic hematuria, digital gangrene, and progressive interstitial lung disease)
  • •Having unstable cardiopulmonary disease (angina, peripheral vascular disease, cerebrovascular disease, and arrhythmia) and risk of cardiovascular disease
  • •Having a history of schizophrenia, concurrent active mood disorder, or anxiety disorders
  • •Receiving the following medications that cause drug interaction with cannabinoids: fluoroquinolone, rifampicin, fluoxetine, warfarin

研究组 & 干预措施

placeba

Placebo Comparator

Placebo 1 droplet twice daily for 1 week then titrate up to 2 droplets twice daily if tolerated and continue the treatment until the end of the study

干预措施: Placebo (Drug)

cannabinoid

Experimental

Cannabinoid in form of cannabis 2.7 mg THC 2.5 mg twice daily (1 droplet twice daily; 0.73 mg THC and 0.81 mg CBD/drop, 1.46 mg THC and 1.62 CBD/day) for 1 week then titrate up to 2 droplets twice daily if tolerated (2.92 mg THC and 3.24 CBD per day) and continue the treatment until the end of the study

干预措施: CBD oil (Drug)

结局指标

主要结局

The changing of appetite

时间窗: 4 weeks

50% increase of appetite evaluated by a visual analogue scale (VAS) from 0-100\* compared to baseline and a comparison between the treatment group and placebo group \*a higher score, a more appetite

次要结局

  • An adverse event(4 weeks)
  • The changing of serum transferrin level(4 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Chingching Foocharoen

Professor

Khon Kaen University

研究点 (2)

Loading locations...

相似试验