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Safety of Etoricoxib and Piroxicam oral drugs in Osteoarthritis patients at Rama hospital Kanpur

A comparative study to evaluate the safety & efficacy of Etoricoxib and Piroxicam in pharmacotherapy of Osteoarthritis in tertiary care hospital Kanpurâ??â??

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/12/047816
Enrollment
290
Registered
2022-12-01
Start date
Unknown
Completion date
Unknown
Last updated
2023-01-09

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

Conditions

Health Condition 1: M179- Osteoarthritis of knee, unspecified

Interventions

Intervention1: Etoricoxib: Tablet. Etoricoxib - 60 mg BD orally for one month. Intervention2: Piroxicam: Tablet. Piroxicam - 20 mg BD orally for one month. Control Intervention1: 1. Etoricoxib 2. Piro

Sponsors

PRINC BGHEAL
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients with symptomatic osteoarthritis of age 35 to 65 years who fulfill the western Ontario and McMaster universities osteoarthritis index (WOMAC) 2. Criterion for the diagnosis of osteoarthritis will be enrolled. 3. Patients having symptomatic Osteoarthritis either as a new case or as an old case following discontinuation of treatment with NSAIDS or other analgesic medications with a washout period of one week 4. All these patients will be examined as per the baseline criteria will be included in the study if they fit this criterion.

Exclusion criteria

Exclusion criteria: 1. Smokers/ alcoholics 2. Pregnant & lactating women. 3. Patients on steroid therapy, history of chronic infections like TB, leprosy, recent trauma, surgery, mental retardation, minor. 4. Patients with liver diseases, kidney diseases, and cardiac problems.

Design outcomes

Primary

MeasureTime frame
1. Pain, Stiffness, physical Function - measured with Western Ontario and McMaster Universities Arthritis Index (WOMAC). 2. Adverse effects: Total number of adverse effects (all), Gastrointestinal adverse effects (for example, nausea, vomiting), Neurological (nervous system) adverse effects (for example, headache, fatigue, dizziness).Timepoint: one month

Secondary

MeasureTime frame
Improvement - measured with a Patient Global Impression Scale of Improvement (PGI) as a quality indicator.Timepoint: one month

Countries

India

Contacts

Public ContactPRINC BGHEAL

RAMA MEDICAL COLLEGE, HOSPITAL AND RESEARCH CENTRE

drnilamnigam@gmail.com9140190476

Outcome results

None listed

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