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Osteoporosis clinical trials

View clinical trials related to Osteoporosis.

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NCT ID: NCT05345691 Active, not recruiting - Clinical trials for Postmenopausal Women With Osteoporosis

Comparison of Efficacy, Pharmacodynamics, Safety, and Immunogenicity Between Bmab 1000 and Prolia® in Postmenopausal Women With Osteoporosis

DEVOTE
Start date: May 24, 2022
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, multicenter, parallel-arm, Phase 3 study to compare the efficacy, PK (Pharmacokinetic), PD (Pharmacodynamic), safety, and immunogenicity of Bmab 1000 and Prolia® in postmenopausal women with osteoporosis

NCT ID: NCT05338086 Active, not recruiting - Clinical trials for Postmenopausal Women With Osteoporosis

A Study to Compare Efficacy, Pharmacokinetics, Pharmacodynamics, Safety and Immunogenicity of MB09 [Proposed Denosumab Biosimilar] to Prolia® [EU-sourced] in Postmenopausal Osteoporosis (SIMBA Study)

Start date: March 31, 2022
Phase: Phase 3
Study type: Interventional

This is a randomized, double-blind, parallel, multicenter, multinational study to compare the efficacy, pharmacokinetics, pharmacodynamics, safety and immunogenicity of MB09 versus Prolia® in postmenopausal women with osteoporosis

NCT ID: NCT05332626 Active, not recruiting - Bone Loss Clinical Trials

Lactobacillus Acidophilus and Postmenopausal Osteoporosis Women

LaBon
Start date: February 1, 2022
Phase: N/A
Study type: Interventional

This study aims to evaluate the effect of Lactobacillus acidophilus supplementation on calcium status and bone densitometry in postmenopausal women in a randomized, double-blind placebo-controlled study.

NCT ID: NCT05326815 Active, not recruiting - Osteoporosis Clinical Trials

A Comparison of Serum and Urine N-telopeptide Marker

Start date: March 28, 2022
Phase:
Study type: Observational

This is a prospective specimen collection cohort study to evaluate the correlation between serum and urine values of the bone marker of interest, and their association with baseline DEXA scan measures and fracture risk within 6 months. Study samples will be obtained longitudinally. One collection of both serum and urine collection will be obtained. The urine will be collected as second void of day and at the same time the blood collection is drawn. Study will continue for a period or 1 year, with plan to enroll around 40 subjects.

NCT ID: NCT05283148 Active, not recruiting - Osteoporosis Clinical Trials

Sickle Cell Disease (SCD) Bone Pain Study

Start date: November 3, 2022
Phase: N/A
Study type: Interventional

A prospective study to determine how low bone mineral density and/or vertebral compression fractures associate with pain in adults with sickle cell disease

NCT ID: NCT05101018 Active, not recruiting - Osteoporosis Clinical Trials

Treatment With Romosozumab Versus Denosumab to Improve Bone Mineral Density and Architecture in Subacute SCI

Start date: November 1, 2021
Phase: Phase 4
Study type: Interventional

The objective of the proposed work is to determine whether administration for 12 months of romosozumab followed by 12 months of denosumab will maintain bone mass at the knee in subjects with subacute SCI compared to 24 months of denosumab administration alone.

NCT ID: NCT05016310 Active, not recruiting - Breast Cancer Clinical Trials

A Study of High-Dose Vit D Versus Standard of Care Vit D Supplementation

Start date: September 16, 2021
Phase: N/A
Study type: Interventional

This is a randomized study evaluating the effects of early intensive vitamin D supplementation compared to standard of care vitamin D supplementation on bone health over an 18 month period.

NCT ID: NCT05010590 Active, not recruiting - Clinical trials for Postmenopausal Osteoporosis

Anabolic Therapy in Postmenopausal Osteoporosis

Start date: March 24, 2022
Phase: Phase 4
Study type: Interventional

In this research study we want to learn more about the effect of two different FDA-approved medications in the treatment of osteoporosis.

NCT ID: NCT04785131 Active, not recruiting - Osteoporosis Risk Clinical Trials

Prune Consumption and Bone Health in Young Women Using Hormonal Contraceptives

Start date: November 30, 2019
Phase: N/A
Study type: Interventional

The primary objective of this study is to determine if 12 months of consuming 50 grams of dried plum daily will prevent bone loss or augment bone accrual of young adult oral contraceptive (OC) users.

NCT ID: NCT04708886 Active, not recruiting - Osteoporosis Clinical Trials

Romosozumab in Women With Chronic SCI

Start date: March 1, 2021
Phase: Phase 2
Study type: Interventional

This two-year open-label pilot clinical trial will evaluate the efficacy and safety of romosozumab to treat bone loss in females with chronic spinal cord injury (SCI) and osteoporosis (OP). Participants will receive monthly injections of romosozumab during the first 12 months of the study. During the second year, participants will take oral alendronate tablets on a weekly basis.