Phase IV Post-Marketing Surveillance Study to Measure the Efficacy and Safety of Dr.Ortho Pain Relief Oil in Subjects Suffering from Acute Sports Injury, Knee Pain, Stiffness in Joints, Lower Back Pain, Neck Rigidity, Backache and Inflammation in Joints
Phase 4
- Conditions
- Health Condition 1: M959- Acquired deformity of musculoskeletal system, unspecified
- Registration Number
- CTRI/2021/07/034542
- Lead Sponsor
- Divisa Herbal Care
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Closed to Recruitment of Participants
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Age Between 18 - 80 Years
2.Subjects suffering from Knee pain and joint pain and arthritis
3. Willingness to Take part in Study and able to attend all Scheduled Visits
4.Subjects suffering from Acute sports injury, strains, sprain, chronic Arthritis, back pain, knee pain, and other joint pain
Exclusion Criteria
1.Pregnant, Breastfeeding, subjects undergone any surgery and else take taken part in any clinical Trial
2.Not willing to Sign the ICF or give the consent
Study & Design
- Study Type
- PMS
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. To assess the percentage of subjects with significant symptomatic reduction of joint muscle stiffness, neck rigidity, and backache assessed through Investigator Assessment Scale and Subject Assessment QuestionnairesTimepoint: Day 1 to day 30
- Secondary Outcome Measures
Name Time Method 1.Improvement in the VAS scoring on the successive application as compared to baseline <br/ ><br>2.Incidence of any AEs during the studyTimepoint: Day 1 to day 30