A randomized double-blinded comparative efficacy study of TF1 and TF2 in Adult Subjects with exercise induced acute musculoskeletal pain - Nil

Arjuna Natural Private Ltd0 个研究点目标入组 60 人开始时间: 待定最近更新: 2023年10月16日

试验速览

暂无简介。

•Adult subject, Male or female between 18-65 years of age.
•A score of 5 or above on the NRS.
•Subjects having exercise induced acute musculoskeletal pain which occurred within 24 hours before presentation.
•Willing to give voluntary informed consent.

•Subject with acute muscle spasms who need parenteral therapy, surgery or hospital admission for management, painful uncomplicated acute soft tissue injury of the upper or lower extremity, including acute injuries of ligaments, tendons, or muscles. Subjects with Grade 2 & 3 sprain or strain or muscle cramps due to dehydration.
•Pain originating from bone.
•Subjects with known history of osteoarthritis and rheumatoid arthritis.
•Subjects with open wounds infected skin or other conditions of broken skin, skin affected by infection with inflammations at the site of proposed action.
•Use of any oral or topical analgesic, antipyretic, sedative or anti-inflammatory treatment, Use of any topical products, including topical medications, sunscreens, lotions, moisturizers, and cosmetic products at the site of pain within 1 week prior study or during the study.
•Any kind of neuralgic pain, headache and/or chronic pain
•Previous adverse reaction or known allergy to herbal, NSAID, steroids or any other severe food allergies.

发起方

Arjuna Natural Private Ltd