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A randomized controlled study of postoperative residual pain after vertebroplasty for osteoporotic vertebral compression fractures treated with Fu’s Subcutaneous Needling based on the theory of the tightened muscle

A randomized controlled study of postoperative residual pain after vertebroplasty for osteoporotic vertebral compression fractures treated with Fu’s Subcutaneous Needling based on the theory of the tightened muscle

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087270
Enrollment
Unknown
Registered
2024-07-24
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-07-29

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

Conditions

postoperative residual pain after vertebroplasty for osteoporotic vertebral compression fractures

Interventions

FSN therapy group:Fu’s Subcutaneous Needling (Treatment once a day, a total of 7 treatments)+ Meloxicam tablets
Control Group:Meloxicam tablets, 7.5mg(1 tablet) once daily

Sponsors

Suining Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to No maximum

Inclusion criteria

Inclusion criteria: (1) Meets the diagnostic criteria for osteoporotic vertebral compression fractures in the Expert Consensus on the Diagnosis and Treatment of osteoporotic vertebral compression Fractures (2021 edition); (2) Aged 50 years and over; (3) VAS score >= 4 points; (4) Lower back pain was still present, 24 hours after percutaneous vertebroplasty (PVP)/percutaneous kyphoplasty (PKP); (5) Palpation of soft tissues in the low back was "tight, stiff, hard and slippery", accompanied by local pain; (6) Volunteer to participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Patients with other injuries or fractures to the lower back, prior spinal surgery, or spinal malformations. (2) Patients with metastatic tumor, spinal infection,metabolic bone disease, including primary parathyroid hormone bone disease, renal bone disease, toxic bone disease; (3) Combined with other chronic diseases or other neurological disorders that cause low back pain; (4) Patients with uneven distribution of bone cement, bone cement leakage and multiple vertebral fractures after PVP/PKP; (5) Patients with severe back skin injury, postoperative incision swelling, exudation, and bleeding tendency; (6) Serious cardiovascular and cerebrovascular diseases, digestive system diseases, liver and kidney function abnormalities, and blood system diseases; (7) Suffer from mental and psychosomatic diseases, such as anxiety and depression; (8) Those with poor compliance do not want to participate.

Design outcomes

Primary

MeasureTime frame
Pain;Temperature at the site of pain;

Secondary

MeasureTime frame
Oswestry;Japanese Orthopaedic Association(JOA);Levels of serum inflammatory factors;

Countries

China

Contacts

Public ContactWang Qiong

Suining Central Hospital

joantcm@163.com+86 199 0805 7065

Outcome results

None listed

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