Blood Stasis Type Osteoporosis-related Pain
Conditions
Interventions
Control Group:Routine intervention
Observation group:Routine intervention + Liumo Analgesic Beverage
Sponsors
Xi'an City Traditional Chinese Medicine Hospital
Eligibility
Sex/Gender
All
Age
45 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1. Agree to participate in this clinical trial and sign the informed consent form; 2. Meet the Western diagnostic criteria for primary osteoporosis; 3. Be diagnosed with blood stasis syndrome according to traditional Chinese medicine; 4. All patients have pain in the waist, back, or joint areas, with a pain duration of =3 months.
Exclusion criteria
Exclusion criteria: 1. Individuals who have experienced a fracture within the past six months 2. Those with concurrent endocrine or metabolic disorders (hyperparathyroidism, Cushing's syndrome, hyperthyroidism, hypergonadism, diabetes), hematologic disorders (myeloma, leukemia), severe gastrointestinal diseases, and mental or neurological disorders, etc 3. ; 4. Individuals with severe cardiovascular diseases or impaired liver or kidney function 5. Patients with mental disorders 6. Those participating in other clinical trials or who have completed participation in other drug clinical trials within the past three months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Bone Density Measurement;Pain score;Bone turnover markers: ß-CTX, PINP;Inflammatory factors: TNF-alpha, IL-1; | — |
Secondary
| Measure | Time frame |
|---|---|
| Blood Stasis Syndrome Scoring;Serum MCV, RDW-CV, MPV, PDW; | — |
Countries
China
Contacts
Public ContactWang Hui
Xi'an City Traditional Chinese Medicine Hospital
Outcome results
None listed