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NCT05402852

Effectiveness and Safety of EuBone® Capsules for Bone Health in Postmenopausal Women

Status unknown Phase 4 Last updated 2 June 2022
What this trial tests

Phase 4 trial testing EuBone ® capsule in Osteoporosis, Postmenopausal in 30 participants. Status unknown.

Timeline
1 June 2022
Primary endpoint
31 October 2022
31 December 2023

Quick facts

Lead sponsorShandong University
PhasePhase 4
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingtriple
Primary purposetreatment
Enrollment30
Start date1 June 2022
Primary completion31 October 2022
Estimated completion31 December 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Shandong University

Who can join

Adults 45 to 75, female only, with Osteoporosis, Postmenopausal. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

EuBone is prepared by mixing eucommia ulmoides extract, fructus ulmoides extract and dodder extract in proportion. The aim of this study is to evaluate the effectiveness and safety of EuBone® capsules in slowing bone loss, preventing bone loss, and improving quality of life compared with placebo in Postmenopausal women.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Osteoporosis, Postmenopausal

Currently open trials in the same condition.

Other Shandong University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

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