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Post-Marketing Drug Intensive Monitoring Surveillance of EDIROL in Patients With Postmenopausal Osteoporosis

Postmenopausal Osteoporosis Clinical Trial

Official title:
EDIROL Drug Intensive Monitoring: Post-Marketing Drug Intensive Monitoring Surveillance of EDIROL in Patients With Postmenopausal Osteoporosis

Clinical Trial Summary

This is a post-marketing drug intensive monitoring surveillance with an observational, non-interventional design. The objectives are to compare the incidence of hypercalcemia in patients with and without calcium intake (including dietary supplements, excepting calcium from meals), and to monitor the type, incidence, severity, and relevance of other adverse drug reactions,including urolithiasis.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05433207
Study type Observational
Source Chugai Pharmaceutical
Contact Ritsu Ki
Phone only use E-mail
Email edrdimdisclosure@chugai-pharm.co.jp
Status Not yet recruiting
Phase
Start date August 1, 2022
Completion date January 31, 2025
View Details
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