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Risk of hypercalcemia with calcium/active vitamin D supplementation in teriparatide treatment of severe osteoporosis

Risk of hypercalcemia with calcium/active vitamin D supplementation in teriparatide treatment of severe osteoporosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400087449
Enrollment
Unknown
Registered
2024-07-26
Start date
2024-08-01
Completion date
Unknown
Last updated
2025-11-03

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

Conditions

osteoporosis

Interventions

teriparatide alone group:None
combined calcium supplements group:None
combined active vitamin D group:None
combined calcium supplements and active vitamin D group:None

Sponsors

Shanghai Sixth People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
45 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1.Postmenopausal osteoporotic women with =1 year of menopause 2. Bone mineral density T-value <-3.0 in the lumbar spine, femoral neck, or total hip; or at least one osteoporotic fracture after menopause 3.Treatment with teriparatide 4. Available pre-dose biochemical test results and followed up at least once at 3 months, 6 months, or 1 year post-dose.

Exclusion criteria

Exclusion criteria: 1. Intravenous bisphosphonates within 1 year 2. Use of desutumumab within 6 months 3. Have other metabolic bone disease (e.g. osteochondrosis, osteogenesis imperfecta, Paget's disease) 4. Unwilling to participate in the study

Design outcomes

Primary

MeasureTime frame
serum calcium;

Secondary

MeasureTime frame
bone density;Serum procollagen type I N-terminal propeptide;Serum osteocalcin;Serum type ? collagen C-terminal peptide crosslinking;

Countries

China

Contacts

Public ContactYue Hua

Shanghai Sixth People's Hospital

yueyinglonghua@163.com+86 189 3017 2517

Outcome results

None listed

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