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Safety and Efficacy of Arthronat in subjects with painful Osteoarthritis

Randomized, double blind, parallel group, placebo controlled study to evaluate the safety and efficacy of Arthronat in subjects with painful Osteoarthritis of hips, knees, shoulders, neck or wrists

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2011/07/001886
Enrollment
80
Registered
2011-07-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Osteoarthritis

Interventions

Intervention1: Arthronat: 1500 mg (500mg X 3) 2 times in a day for 4 weeks Control Intervention1: Placebo: 3 capsules 2 times in a day for 4 weeks

Sponsors

Rowtasha
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: A previously diagnosed (atleast 3 months prior to the screening visit) case of osteoarthritis of hip, knees based on the ACR Clinical Classification criteria for osteoarthritis A previously diagnosed (atleast 3 months prior to screening visit) case on shoulders, neck and wrists based on the clinical and radiographic findings.

Exclusion criteria

Exclusion criteria: Subject with history of disease which may involve the index joint including but not limited to rheumatoid arthritis Any inflammatory joint disease Metabolic bone disease (gout, pseudo gout etc) Bone tumours Joint infections (reactive arthritis, septic arthritis) Avascular necrosis (especially of neck of femur) Neuropathic disorders etc.

Design outcomes

Primary

MeasureTime frame
Change in the pain scores as evaluated by Visual Analogue Scale (VAS) at end of 1 week as compared to Baseline (Day 0 / Visit 2) Improvement (change) in mobility at the end of Week 1 as compared to Baseline (day 0 / Visit 2) evaluated by change in the WOMAC sub-scales of Stiffness and Physical function.Timepoint: 1 Week

Secondary

MeasureTime frame
Change in the pain scores as evaluated by VAS at end of 2, 3 and 4 weeks as compared to Baseline (Day 0 / Visit 2)Timepoint: week 2, 3 and 4

Countries

India

Contacts

Public ContactKarthik C
girisha.r@ecronacunova.com080-66915700

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026