跳至主要内容
临床试验/RPCEC00000171
RPCEC00000171已完成4 期

Effects of the administration of Abexol (D-002) and Prevenox (D-003) in subjects with osteoarthritis symptoms

Center of Natural Product / National Center for Scientific Research0 个研究点目标入组 120 人开始时间: 2013年9月20日最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
120

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomized controlled trial. Masking: Double Blind. Control group: Placebo. Assignment: Parallel. Purpose: Treatment

入排标准

年龄范围
20 years 至 80 years(—)
性别
All

入选标准

  • The sample will be made ??up of:
  • 1. Women and men.
  • 2. Ages between 20 and 80 years.
  • 3. With symptoms of OA (joint pain in hip, spine, limbs and / or phalanges).
  • 4. Which have agreed to give informed consent.
  • 5. Patients classified in Scales I-III of the American Association of Rheumatology.
  • 6. Patients with WOMAC score = 25.

排除标准

  • 1. Existence of other forms of arthritis.
  • 2. Arthroplasty in the last 3 years.
  • 3. Any orthopedic surgery in the last 3 years.
  • 4. Transplanted.
  • 5. Active liver or kidney diseases.
  • 6. Neoplasms diagnosed.
  • 7. Severe high blood pressure
  • 8. Uncompensated diabetes mellitus (fasting glucose> 7 mmol / L).
  • 9. Hospitalization for any cause in the previous 6 months.
  • 11. Subjects with normal clinical history of allergy to any other medicines
  • 12. Subjects with other special conditions that endanger their health and their lives during the study.

研究者

发起方
Center of Natural Product / National Center for Scientific Research

相似试验