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Eldecalcitol and Calcitriol in Postmenopausal Women With Low Bone Mineral Density or Mild Osteoporosis — EFFECT  

Postmenopausal Osteoporosis Clinical Trial

Official title:
Comparison of the Efficacy and Safety With Eldecalcitol and Calcitriol in Postmenopausal Women With Low Bone Mineral Density or Mild Osteoporosis

Clinical Trial Summary

To investigate the efficacy and safety of eldecalcitol in postmenopausal women with low bone mineral density (BMD) or mild osteoporosis through a randomized, open-label, parallel controlled trial with calcitriol as the control.

Clinical Trial Description

Postmenopausal women with low bone mineral density (BMD) or mild osteoporosis will be randomized in a 1:1 ratio to receive open-label oral 0.75μg eldecalcit daily or open-label oral 0.5μg calcitriol daily for 12 months. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05902078
Study type Interventional
Source Shanghai Jiao Tong University Affiliated Sixth People's Hospital
Contact Li Shen
Phone (+86)15800674978
Email shenli_0510@126.com
Status Recruiting
Phase Phase 4
Start date September 27, 2023
Completion date December 2025
View Details
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