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Translation to English: **"Evaluation of the Pain-Control Effect of Piroxicam Nanotransfersomal Emulgel in Osteoarthritis and Rheumatoid Arthritis"**

Evaluation of the performance of an emulgel containing piroxicam-loaded nano transferosome for controlling knee joint pain in patients with osteoarthritis and rheumatoid arthritis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180526039839N2
Enrollment
100
Registered
2026-05-21
Start date
2026-06-22
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Chronic pain and mobility function of knee joint pain. Pain in joint

Interventions

Intervention 1: Control group: Piroxicam Gel (0.5%). Intervention 2: Intervention group: Piroxicam Gel (0.5%)+Nanotransfersomal Piroxicam Emulgel.

Sponsors

Daroosazan Sorena Exir Pharmaceutical Company
Lead Sponsor

Eligibility

Sex/Gender
All
Age
25 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients diagnosed with osteoarthritis or rheumatoid arthritis presenting pain in one or both knee joints Chronic knee joint pain persisting for more than 3 months Non-responsiveness to initial oral or topical treatments (including standard medications). Willingness and informed consent to participate in the study

Exclusion criteria

Exclusion criteria: Use of any analgesic medications (oral, injectable, or suppository forms), including acetaminophen, nonsteroidal anti-inflammatory drugs (NSAIDs), narcotics, or herbal products with proven analgesic activity (e.g., black seed oil) during the 7-day study period or in the weeks preceding the study Known hypersensitivity or allergy to piroxicam or any components of the emulgel formulation Presence of active wounds or skin lesions on the knee area Severe systemic diseases that may influence study outcomes Pregnancy or lactation Inability or unwillingness to cooperate or complete questionnaires required in the study

Design outcomes

Primary

MeasureTime frame
Pain level in knee joint. Timepoint: The pain level is measured every 24 hours. Method of measurement: The pain is evaluated based of emotional, perceptional and sensational variables of McGill questionnaire.

Secondary

MeasureTime frame
Pain level at rest and function. Timepoint: Evaluation every 24 hours. Method of measurement: Evaluation with McGill or VAS.;Onset of painkilling action. Timepoint: every 24 hours. Method of measurement: Record of onset of action (insight of patient/volunteer).;Systemic/topical adverse effects/reactions. Timepoint: Every 24 hours. Method of measurement: Patient/volunteer insight survey.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammad Ali Nazarinia

Shiraz University of Medical Sciences

Hafezhospt@sums.ac.ir+98 71 3647 9531

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026