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Clinical study for probiotics on osteoporosis

Clinical study for probiotics on osteoporosis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800019268
Enrollment
Unknown
Registered
2018-11-02
Start date
2018-11-02
Completion date
Unknown
Last updated
2018-11-05

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

Conditions

osteoporosis

Interventions

Experimental group:Conventional medicines+probiotics
Control group:Conventional medicines+placebo

Sponsors

The Affiliated Hospital of Inner Mongolia Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
55 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) patients whose t-value of bone mineral density is less than -1; (2) no combined endocrine and metabolic diseases (hyperthyroidism, Cushing's syndrome, hypogonadism, hyperthyroidism, pituitary prolactin tumor, diabetes (mainly in type 1 diabetes and part of type 2 diabetes), and hypophysis); Connective tissue disease (systemic lupus erythematosus (sle) and sjogren's syndrome, dermatomyositis, mixed connective tissue disease), a variety of chronic kidney disease causes renal osteodystrophy, gastrointestinal disease and nutritional diseases (malabsorption syndrome, gastric bowel resection most, chronic pancreatic diseases, chronic liver disease, malnutrition, chronic venous nutrition support treatment), and blood system diseases (leukemia, lymphoma, multiple myeloma and abnormal bone marrow proliferation syndrome), neuromuscular system disease (of hemiplegia caused by various reasons, paraplegia, motor dysfunction, muscular dystrophy, jiang syndrome and myotonia syndrome), brake for a long time Or patients with osteoporosis after space travel, organ transplantation, drugs and poisons (immunosuppressants, heparin, anticonvulsants, cancer drugs, aluminum antacids, thyroid hormones, chronic fluorosis, gonadotropin releasing hormone agonist (gnrh-a) or renal failure dialysis).

Exclusion criteria

Exclusion criteria: 1. Secondary osteoporosis (with endocrine metabolic disorders, connective tissue disease, a variety of chronic kidney disease causes renal osteodystrophy, gastrointestinal disease and nutritional diseases, blood system diseases, diseases of the neuromuscular system, brake for a long time or space travel, organ transplantation, drugs and poisons;) in patients with osteoporosis; 2. Active stage of peptic ulcer; 3. Patients with malignant gastrointestinal neoplastic disease; 4. Previous cases of lactose intolerance, irritable bowel syndrome, inflammatory bowel disease, habitual diarrhea and other intestinal diseases; 5. Patients with infectious diseases need to be treated with antibiotics; 6. Have a history of allergy to lactobacillus and its products or a hypersensitive constitution; 7. Other researchers consider it inappropriate to participate in this study.

Design outcomes

Primary

MeasureTime frame
Bone mineral density;

Countries

China

Contacts

Public ContactZhao Jianmin

The Affiliated Hospital of Inner Mongolia Medical University

nmzjmin@163.com+86 13604719169

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 13, 2026