Abaloparatide Before Total Knee Arthroplasty

Status Active, not recruiting

Clinical Trial Summary

The investigator hypothesizes that treating osteoporotic patients with abaloparatide prior to and after total knee arthroplasty will significantly reduce the amount of bone loss.

Clinical Trial Description

In primary unilateral total knee arthroplasty patients, The investigator will examine the effect of daily abaloparatide therapy in clinical osteoporotic patients beginning 3 months pre-op and continued for a total of 15 months. This will be compared to osteopenic patients receiving no therapy as well as previously published values in untreated osteoporotic patients 12 months following Total Knee Arthroplasty (TKA). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04167163
Study type	Interventional
Source	University of Wisconsin, Madison
Contact
Status	Active, not recruiting
Phase	Phase 4
Start date	January 10, 2020
Completion date	March 2025

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