Skip to content

Comparing the effect of calcitonin mesotherapy versus peri-articular prolotherapy in Reducing Pain and Improving Function in patients with knee osteoarthritis

Comparing the effect of calcitonin mesotherapy versus peri-articular prolotherapy in Reducing Pain and Improving Function in patients with knee osteoarthritis (randomized clinical trial)

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20241219064100N1
Enrollment
64
Registered
2025-01-20
Start date
2025-02-28
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

knee osteoarthritis. Primary generalized (osteo)arthritis

Interventions

Intervention 1: Intervention group A : The treatment for group A will be mesotherapy, which involves injecting a mixture of 2 ml of 2% lidocaine and 100 units of calcitonin on days 1, 8, and 15. This

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 70 Years

Inclusion criteria

Inclusion criteria: Presence of pain and other clinical symptoms of knee osteoarthritis within the past month Age between 40 and 70 years Absence of any disease around the affected joint

Exclusion criteria

Exclusion criteria: Diabetes rheumatic and collagen vascular diseases and gout and lupus Concurrent radiculopathy Nerve injury and neuropathies Brucellosis Body mass index greater than 42 History of knee replacement in the affected side History of trauma and fracture of the affected joint Bleeding disorders Inability to communicate and complete questionnaires History of allergy and hypersensitivity reactions to the medications used History of significant liver, kidney, and cardiopulmonary disorders History of intra-articular or periarticular injections in the affected joint within the past 3 months Pregnant women Lower extremity deformities Individuals with cancer Individuals using anticoagulant medications

Design outcomes

Primary

MeasureTime frame
Reducing pain and improving patient function. Timepoint: Assessing the level of knee pain in patients before the injection and in the second, fourth, eighth, and twelfth weeks after the injection, as well as completing the VAS, WOMAC, and OKS questionnaires before the injection and in the second, fourth, eighth, and twelfth weeks after the injection. Method of measurement: The Western Ontario and McMaster Universities Arthritis Index and Visual Analogue Scale and Oxford Knee Score.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDaniyal Emami

Shiraz University of Medical Sciences

info@sums.ac.ir+98 71 3212 2710

Outcome results

None listed

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