跳至主要内容
临床试验/CTRI/2022/11/047233
CTRI/2022/11/047233已完成未知

An Openâ??Label, Two Group Clinical Study to Evaluate the Efficacy and Safety of HRUP-122101in Acute Musculoskeletal Pain or Acute Sports Injury Pain Relief

Himalaya Wellness Company0 个研究点目标入组 104 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
104

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Adults of either gender aged >=18 - <=65 years and children of either gender aged >=12 - <= 17 years.
  • 2. Subjects with acute musculoskeletal pain (Back ache, joints pain, neck pain, shoulder pain etc.), sprain, strains and/ or acute sports injury pain.
  • 3. Subjects willing to sign informed consent/assent form and follow with the schedule.
  • 4. Subjects who have not participated in similar kind of study in last 4 weeks. 5. Parents/ Guardians/ Caregivers of the children of aged >=12- <= 17 willing to sign written consent (as applicable) and follow the study procedure. Children also should be giving the written assent

排除标准

  • Subjects with chronic pain like arthritis, gout, ankylosing spondylitis.
  • 2. Subjects suffering from auto-immune disorders, spastic disorders, genetic disorders, and severe traumatic conditions.
  • 3. Any evidence or history of hypersensitivity to any of the components in the HRUP-122101.
  • 4. Any known skin disorder or presence of open wounds.
  • 5. Subjects who are taking any additional topical therapy or systemic NSAIDs.
  • 6. Clinical diagnosis of bruised, trauma, muscle damage.
  • 7. Subjects with raw wounds, sutures, fractures, and hematoma.
  • 8. Pregnant or lactating women/ women not willing to follow adequate standard contraceptive measures.

研究者

相似试验