Effect of Elartrit in knee osteoarthritis

Not Applicable

Recruiting

• Conditions: Knee osteoarthritis.; Osteoarthritis of knee, unspecified; M17.9

• Registration Number: IRCT20220502054724N1
• Lead Sponsor: Shiraz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 29 August 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 60

Inclusion Criteria

Filling and signing the consent form
Having pain and other clinical manifestations of knee osteoarthritis in the last month
Being between 40 to 60 years old
Not having any periarticular disease around the joint in question

Exclusion Criteria

High grade arthritis according to radiology
Presence of diabetes mellitus
Presence of rheumatologic and collagen vascular diseases such as gout and lupus
Presence of concomitant radiculopathy
Presence of neural damage and neuropathy
Presence of brucellosis
Presence of any malignancy
Presence of a history of significant liver disease
Presence of a history of significant liver disease
Presence of a history of significant kidney disease
Presence of a history of significant cardiac disease
Presence of a history of significant pulmonary disease
A body mass index greater than 42
Presence of a history of knee joint replacement in the knee being studied
Presence of a history of trauma or fracture in the knee being studied
Presence of bleeding disorders
Presence of an inability to communicate and to complete questionnaires
Presence of a history of allergic or hypersensitivity reaction to the drugs being used
Presence of a history of injections in the last 3 months within or around the joint being studied
Presence of a state of pregnancy or lactation
Patients taking anticoagulant medications
Presence of a history of gastrointestinal and stomach disease
Use of warfarin and ticlopidine

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Pain caused by knee osteoarthritis. Timepoint: Before starting the intervention; 2, 4, and 8 weeks later. Method of measurement: Visual analog scale; Western Ontario and McMaster Universities Arthritis Index; Oxford knee scale; Patient satisfaction.

Secondary Outcome Measures

Name	Time	Method
Degree of knee dysfunction. Timepoint: Before starting the intervention; 2, 4, and 8 weeks later. Method of measurement: Western Ontario and McMaster Universities Arthritis Index; Oxford knee scale; Patient satisfaction.