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临床试验/CTRI/2023/07/055689
CTRI/2023/07/055689尚未招募4 期

A Clinical Study to Evaluate the Safety and Efficacy of Panchakarma Essential (Nirgundi-based formulation) in reducing symptoms of Knee Osteoarthritis. - NI

Mprex Healthcare Pvt. Ltd.0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
尚未招募

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

  • 1. Male and female subjects 30-60 years of age (both inclusive)
  • 2. The patient diagnosed with an OA of the knee for greater than 3 months
  • 3. VAS (visual analog scale) score during the most painful knee movement between 40-70 mm.
  • 4. Subjects with or without consuming analgesics and anti-inflammatory medicines.
  • 5. Willing to refrain from taking ibuprofen, aspirin, other NSAIDs, or any other pain reliever (OTC or prescription) during the entire trial.
  • 6. Ambulatory subject able to provide verbal and written consent and ready to comply with all study procedures.

排除标准

  • 1. Female subjects, who are pregnant, breastfeeding, or planning to become pregnant.
  • 2. Recent injury in the area affected by OA of the knee (past 4 months)
  • 4. History of underlying inflammatory arthropathy or severe OA (VAS score greater than 70)
  • 5. Have taken any intra-articular treatment/injections with a corticosteroid or hyaluronic acid within 6 months preceding the treatment period.
  • 6. History of psychiatric disorder that may impair the ability of subjects to provide written informed consent
  • 7. Participation in any osteoarthritis related trials involving investigational products within 30 days prior to the screening Visit.

研究者

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