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Clinical observation of ultrasound-guided paravertebral injection combined with intramuscular injection of ecalcitonin in rapid relief of osteoporotic low back pain

Clinical observation of ultrasound-guided paravertebral injection combined with intramuscular injection of ecalcitonin in rapid relief of osteoporotic low back pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600123766
Enrollment
Unknown
Registered
2026-04-29
Start date
2025-05-09
Completion date
Unknown
Last updated
2026-05-04

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

Conditions

Osteoporotic low back pain

Interventions

Trial Group:Ultrasound-guided paraspinal nerve injection (Triamcinolone acetonide injection 0.5mg + Lidocaine hydrochloride injection 2.5mg, 5ml per segment, up to 4 segments, once weekly for 2 sessio
Control Group:Intramuscular calcitonin injection (10 units per dose, once weekly for 3 months)

Sponsors

Affiliated Hospital of Jiangsu University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. The diagnostic criteria for primary OP comply with the diagnosis and treatment guidelines for primary OP formulated by the Chinese Medical Association; 2. Low back pain; 3. The course of disease is >=3 months; 4. Conservative treatments such as non-steroidal anti-inflammatory drugs and physical therapy cannot relieve pain; 5. Pain VAS score is >=4 points (i.e., 1-3 is mild, 4-6 is moderate, and 7-10 is severe); 6. Agree to this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients with fresh spinal fractures and radiculopathy; 2. Concurrent with other spinal diseases (such as spinal stenosis, infection, tumor); 3. Having previously received other bone resorption inhibitors or bone formation promoters; 4. Severe impairment of important organ functions and abnormal coagulation function, puncture site infection; 5. Previous allergy to calcitonin drugs; 6. Fasting blood sugar > 10 mmol/L.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale;Oswestry Disability Index;Lumbar forward flexion range of motion;

Secondary

MeasureTime frame
Liver and kidney function;Calcium concentration;Adverse reactions;Withdrawal rate after half a year of treatment;

Countries

China

Contacts

Public ContactLi Chunye

Affiliated Hospital of Jiangsu University

372098744@qq.com+86 132 1839 8733

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 7, 2026