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Effect of Alendronate 70mg Formulation on Bone Turnover Markers and Patient Reported Outcomes

Osteoporosis, Postmenopausal Clinical Trial

Official title:
A Non-interventional Two-arm Two-centre, Retrospective/Prospective Study to Compare the Effect of Alendronate 70mg Formulation (Tablet vs Effervescent Tablet) on Bone Turnover Markers and Patient Reported Outcomes

Clinical Trial Summary

Compare the data obtained with two formulations of alendronate 70 mg (tablets vs effervescent tablet for buffered solution) on the change in bone turnover markers, on gastric tolerance and on treatment adherence (including compliance and persistence).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03435094
Study type Observational
Source Labatec Pharma SA
Contact Aurélie TIREFORD, PharmD
Phone +41 22 593 78 54
Email aurelie.tireford@labatec.com
Status Recruiting
Phase
Start date February 25, 2018
Completion date December 1, 2022
View Details
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