Osteoporosis
Conditions
Interventions
Control group:Take calcium carbonate tablets (Caltech)
Intervention group:Taking salmon liquid calcium
Sponsors
Zhongshan Hospital, Fudan University
Eligibility
Sex/Gender
All
Age
50 Years to 80 Years
Inclusion criteria
Inclusion criteria: 1. 50-80 years old; 2. Diagnosed as primary osteoporosis or bone loss (bone density measurement, -2.5<T value<-1.0); 3. The subjects are able to cooperate with intervention, investigation, and follow-up, with clear consciousness and high cooperation; 4. Has not suffered from any known immunodeficiency diseases, metabolic disorders, or digestive abnormalities, such as hypothyroidism, renal dysfunction, gastrointestinal dysfunction, etc; 5. Not taking any medication known to affect bone mineral metabolism recently (such as hormones, diuretics, or antiepileptic drugs, etc.); 6. Not participating in other clinical trials.
Exclusion criteria
Exclusion criteria: 1. Patients with severe osteoporosis who have not shown significant improvement or progression after standardized anti osteoporosis treatment in the past; 2. Liver and kidney dysfunction, or previous severe urinary system stones; 3. Combination of important organ dysfunction and inability to take oral calcium supplements; 4. Researchers believe that subjects who are not suitable for this clinical practice; 5. Individuals with combined mental illnesses or unable to cooperate with corresponding diagnosis and treatment follow-up.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Adverse reaction rate; | — |
Secondary
| Measure | Time frame |
|---|---|
| Rate of bone mineral density remission;Subjective symptom remission rate; | — |
Countries
China
Contacts
Public ContactHuiren Wang
Zhongshan Hospital, Fudan University
Outcome results
None listed