The study of the Treatments with Human-Derived Mesenchymal Stem Cell Conditioned Medium for Pains
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 发起方
- 主要终点
- Impact of pain on daily life
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18age old over 至 No limit（—）
- 性别
- All
入选标准
- •Individuals who did not experience satisfactory pain relief effects with standard therapy.
- •Individuals who are determided by the doctor to be appropriate for receive the treatment with the conditioned medium.
- •<Eligibility Criteria>
- •Patients meeting the following criteria are eligible:
- •Individuals aged 18 years or older.
- •Individuals with normal capacity to consent.
- •Individuals who have been provided with the informed consent document for this treatment, have received sufficient explanation, and are capable of providing written consent freely and voluntarily.
- •Individuals for whom the attending physician has recognized the necessity of treatment.
排除标准
- •<Exclusion Criteria>
- •Individuals meeting any of the following conditions will be excluded:
- •Users of narcotics or stimulants.
- •Individuals who do not have pains except nociplastic pain.
- •Individuals deemed inappropriate by the attending physician.
结局指标
主要结局
Impact of pain on daily life
Assessment of pain (ache) in terms of subjective symptoms of the research participants, evaluating the impact of pain on daily life
Pattern of pain
Assessment of pain (ache) in terms of subjective symptoms of the research participants, evaluating the pattern of pain
Intensity of pain (Numerical Rating Scale; NRS)
Assessment of pain (ache) in terms of subjective symptoms of the research participants, evaluating the intensity of pain using Numerical Rating Scale (NRS)
Location of pain
Assessment of pain (ache) in terms of subjective symptoms of the research participants, evaluating the location of pain
Nature of pain
Assessment of pain (ache) in terms of subjective symptoms of the research participants, evaluating the nature of pain
次要结局
未报告次要终点