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Evaluating the efficacy of duloxetine and gabapentin in pain reduction in patients with knee osteoarthritis

Evaluating the efficacy of duloxetine and gabapentin in pain reduction in patients with knee osteoarthritis

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20170716035126N2
Enrollment
150
Registered
2018-02-17
Start date
2018-03-06
Completion date
Unknown
Last updated
2018-03-26

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

Conditions

Knee osthoarthritis. Osteoarthritis, unspecified site

Interventions

Intervention 1: Intervention group: In Duloxetine group, patients will be treated with 30 mg daily which will be increased to 60 mg daily. Intervention 2: Intervention group: In gabapentine group, tre

Sponsors

Ardabil University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 75 Years

Inclusion criteria

Inclusion criteria: idiopathic knee osteoarthritis Age between 45-75 years ability to walk having pain score of >5 according to VAS and >48 according to WOMAC questionnaire

Exclusion criteria

Exclusion criteria: Other knee disorders Concomitant hip and ankle osteoarthritis Bursitis and perarticular disease radicular pains physiotherapy or intraarticular injection during the past 6 months psychological disease history of knee surgery inflammatory joint disease rheumatoid arthritis fibromyalgia active or recurrent pseudogoat malignancy; systemic diseases including renal of hepatic failure, uncontrolled blood pressure, diabetes mellitus asthma in need of corticosteroids corticosteroid use in less than 5 weeks prior to study

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before intervention and one and three months after intervention. Method of measurement: Using visual analogue scale (VAS).

Secondary

MeasureTime frame
Functional status. Timepoint: Before intervention and one and three months after intervention. Method of measurement: using Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) questionnaire.;Quality of life. Timepoint: Before intervention and one and three months after intervention. Method of measurement: Using SF-12 quality of life questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAfshin Habibzadeh

Ardabil University of Medical Sciences

afshin.habibzadeh@gmail.com+98 45 3352 2391

Outcome results

None listed

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