Osteoporosis, Postmenopausal

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Review clinical trials related to Osteoporosis, Postmenopausal. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effects of Cycle Therapy vs Sequential Therapy With Romosozumab and Denosumab in Postmenopausal Osteoporosis Patients

This study is a prospective, randomized, controlled clinical trial comparing the efficacy of a 24-month cyclic therapy regimen (6 months of Romosozumab followed by 6 months of Denosumab, repeated for two years) versus a traditional sequential treatment regimen (12 months of Romosozumab followed by 12 months of Denosumab). The goal is to determine which approach yields better therapeutic outcomes and to optimize drug strategies for osteoporosis patients.

Participants needed: 70
Trial details
Phase: Phase 4Age: 50-90Biological sex: FemaleType: InterventionalSponsor: National Taiwan University HospitalUpdated: Jun 23, 2026Locations: 1
Eligibility criteria

1. Postmenopausal women aged 50-90 years [+3]

1. Previous osteoporosis treatment within the past two years, including Romosozu... [+12]

Status: Recruiting

Combined Anabolic Therapy

In this research study the study investigators want to learn more about the effect of two different FDA-approved medication regimens in the treatment of postmenopausal osteoporosis.

Participants needed: 50
Trial details
Phase: Phase 4Age: 45+Biological sex: FemaleType: InterventionalSponsor: Massachusetts General HospitalUpdated: Apr 17, 2026Locations: 1
Eligibility criteria

women aged 45+ [+2]

no significant previous use of bone health modifying treatments [+8]

Status: Recruiting

Mechanisms of Anabolic Osteoporosis Therapy

The aim of this study is to investigate the effect of romosozumab on bone cells during early and late phases of treatment.

Participants needed: 16
Trial details
Age: 45+Biological sex: FemaleType: InterventionalSponsor: Massachusetts General HospitalUpdated: Dec 18, 2025Locations: 1
Eligibility criteria

Female aged > 45 years [+2]

renal disease (stage 4 CKD) [+8]

Status: Not yet recruiting

Telerehabilitation Versus Traditional Balance Training in Women With Osteoporosis.

Osteoporosis is a silent disease that leads to fractures, postural deformities, and impaired balance, especially in postmenopausal women. In Pakistan, prevalence is high, with 39% of women reported as severely osteoporotic. Postmenopausal women with osteoporosis and balance issues face increased fall risk due to poor bone density, weakened muscles especially in the lower limb band altered posture .Balance and strength training reduce fall risk, but access to in-person rehabilitation is limited. Telerehabilitation provides remote delivery of structured exercise programs and has shown positive outcomes in balance and bone health. Few studies, however, have compared telerehabilitation with conventional training across all balance domains. The goal of this randomized controlled trial is to compare the effect of Telerehabilitation and Traditional Balance Training in Post Menopausal Women with osteoporosis. Participants will be randomly assigned to one of the two groups, and both will receive an identical standardized balance training program . The results of this clinical trial will help evaluate how telerehabilitation can improve the balance of postmenopausal women with osteoporosis and improve health outcomes.

Participants needed: 60
Trial details
Age: 50-70Biological sex: FemaleType: InterventionalSponsor: Riphah International UniversityUpdated: Dec 1, 2025Locations: 1
Eligibility criteria

• Women diagnosed with osteopenia and osteoporosis at hip and lumbar spine throu... [+4]

• Women with severe mobility impairments. [+2]

Status: Recruiting

Effect of Mechanical Loading and Bone Loss on Motor Neuron Activity-H-Reflex Relationship

Weight-bearing exercises (e.g., running, jumping, whole-body vibration) are widely practiced due to their beneficial effects on bone development and their role in the prevention and treatment of osteoporosis. However, the underlying neuroregulatory mechanisms responsible for these positive effects have not yet been fully understood. Two main neuromodulatory mechanisms have been proposed in the literature: (i) spinal reflexes originating from muscle spindles (stretch reflex, tonic vibration reflex), and (ii) the bone myoregulation reflex (BMR) based on load-sensitive osteocytes. It is well established that increased voluntary contraction and the associated rise in background EMG activity, that is, motor neuron pool activity, enhance muscle spindle-based reflex responses (such as the H-reflex and tendon reflex). In contrast, it has been demonstrated that the H-reflex is suppressed during bone-loading activities such as single-leg stance, jumping, or whole-body vibration. This study is based on two hypotheses: * As mechanical loading increases, Ia inhibitory effects intensify, leading to greater H-reflex suppression. * During whole-body vibration, the H-reflex is suppressed due to Ia inhibition. If this inhibition originates from load-sensitive receptors-osteocytes-and thus from the BMR, then in osteoporosis, where osteocyte number and function are reduced, H-reflex suppression will be diminished. The aim of this research is to test these hypotheses. Confirmation of these assumptions would suggest that reflex control during weight-bearing exercise occurs predominantly through osteocyte-mediated BMR mechanisms rather than muscle spindle-based mechanisms such as the stretch or tonic vibration reflex.

Participants needed: 24
Trial details
Age: 18-65Biological sex: FemaleType: InterventionalSponsor: Istanbul Physical Medicine Rehabilitation Training and Research HospitalUpdated: Nov 28, 2025Locations: 1
Eligibility criteria

Being in the postmenopausal period [+3]

Receiving osteoporosis treatment [+7]

Status: Recruiting

Bone Turnover Markers and Treatment Efficacy in Postmenopausal Osteoporosis

This study investigates the use of blood tests known as Bone Turnover Markers (BTMs) to quickly monitor the effectiveness of osteoporosis treatment in postmenopausal women. Osteoporosis, which weakens bones and increases fracture risk, is typically monitored using a DEXA scan to measure bone density (BMD), but this method changes slowly. BTMs may show a response to medication within just 3 to 6 months. In this randomized controlled trial, 40 postmenopausal women with osteoporosis will be assigned to receive either antiresorptive drugs (which slow bone loss) or anabolic drugs (which build new bone), along with calcium and vitamin D. The study will compare how these treatments affect BTMs and BMD over six months to determine if BTMs can serve as an early and reliable indicator of treatment success, which could be particularly useful in regions like Pakistan where access to repeated DEXA scans is limited.

Participants needed: 40
Trial details
Age: 50+Biological sex: AllType: InterventionalSponsor: Khyber Medical University PeshawarUpdated: Nov 21, 2025Locations: 1
Eligibility criteria

Postmenopausal women (at least one year since last menstrual cycle). [+5]

Women with multiple vertebral fractures or severe lumbar degenerative changes. [+4]

Status: Not yet recruiting

Evaluation of Osteo-Buddy in Improving Osteoporosis Knowledge

This is a pilot randomised controlled trial (RCT) to evaluate the use of a Virtual Health Assistant (VHA) named Osteo-Buddy in improving the knowledge of osteoporosis in older women.

Participants needed: 80
Trial details
Age: 50+Biological sex: FemaleType: InterventionalSponsor: SingHealth PolyclinicsUpdated: Jul 1, 2025
Eligibility criteria

Age 50 and above [+5]

Known terminal illness [+1]

Status: Recruiting

Sequential Therapies After Osteoanabolic Treatment

12-month prospective, open-label, multicenter, international, observational study evaluating sequential treatments after osteoanabolics

Participants needed: 150
Trial details
Age: 50-85Biological sex: FemaleType: ObservationalSponsor: 424 General Military HospitalUpdated: Apr 27, 2025Locations: 8
Eligibility criteria

a bone disease other than postmenopausal osteoporosis [+7]

Status: Recruiting

Single or Repeat Zoledronate Versus Alendronate Following Denosumab (EUROpean Denosumab Effects Consolidation Study)

A 24-month prospective, open-label, randomized, multicenter, multinational, non-inferiority pragmatic clinical trial evaluating zoledronate single or double infusion versus oral alendronate following denosumab

Participants needed: 125
Trial details
Age: 50-85Biological sex: FemaleType: ObservationalSponsor: 424 General Military HospitalUpdated: Apr 27, 2025Locations: 9
Eligibility criteria

a bone disease other than postmenopausal osteoporosis [+6]

Status: Not yet recruiting

Efficacy of OsteoBor in Postmenopausal Osteoporosis

This study aims to evaluate the impact of boron supplementation (OsteoBor) on bone health in postmenopausal women. The trial is a phase 2, randomised, double-blind, placebo-controlled study lasting one year

Participants needed: 30
Trial details
Phase: Phase 2Age: 45-85Biological sex: FemaleType: InterventionalSponsor: Tabriz University of Medical SciencesUpdated: Feb 5, 2025
Eligibility criteria

Not listed

Status: Recruiting

Stress Urinary Incontinence and Sarcopenia in Postmenopausal Osteoporosis

The primary aim of our study is to evaluate the presence of stress urinary incontinence in postmenopausal patients with and without osteoporosis, determine its impact on quality of life, and explore its relationship with sarcopenia.

Participants needed: 100
Trial details
Age: 50-75Biological sex: FemaleType: ObservationalSponsor: Beylikduzu State HospitalUpdated: Dec 12, 2024Locations: 1Duration: 1 Day
Eligibility criteria

Postmenopausal women with DXA measurements performed within the last 6 months. [+1]

Refusal to participate in the study. [+4]

Status: Recruiting

Health Literacy's Impact on Exercise Habits and Medication Adherence in Postmenopausal Osteoporosis

Postmenopausal osteoporosis is characterized by low bone mass and increased fracture risk. Treatment includes exercise, nutrition, supplements, and medications like bisphosphonates, denosumab, or hormone replacement therapy. Lifestyle changes such as quitting smoking, reducing alcohol consumption, and preventing falls are also crucial. Despite effective treatments, adherence is low: 20-30% of patients don't start oral bisphosphonates, and 16-60% continue medications after one year. Exercise adherence rates are similarly low (14.3%-57.7%). This non-adherence imposes a significant clinical and economic burden. Health literacy (HL)-the ability to find, understand, and use health information-is vital for managing health but is understudied in relation to osteoporosis treatment adherence. This study aims to examine the relationship between HL, exercise habits, and medication adherence in postmenopausal osteoporosis patients. Understanding these factors can lead to effective interventions, improving patient adherence and health outcomes. The study will measure HL levels and their correlation with medication and exercise adherence, potentially informing health education programs and strategies to enhance treatment adherence. By doing so, it aims to improve health outcomes and healthcare system efficiency.

Participants needed: 60
Trial details
Age: 45+Biological sex: FemaleType: ObservationalSponsor: Gazi UniversityUpdated: Sep 26, 2024Locations: 1
Eligibility criteria

Postmenopausal patients [+1]

Orthopedic, rheumatic, and neurological conditions that may hinder participation... [+2]

Status: Recruiting

New Biomarkers and Therapeutic Targets in Osteoporosis Via Omics Technologies

This study aims to discover novel biomarkers and therapeutic targets for osteoporosis through the use of advanced omics technologies, including proteomics and metabolomics. By analyzing bone and plasma samples from patients with osteoporosis, the research seeks to understand the underlying mechanisms of the disease and identify potential diagnostic and therapeutic biomarkers.

Participants needed: 60
Trial details
Biological sex: FemaleType: ObservationalSponsor: National and Kapodistrian University of AthensUpdated: Jul 29, 2024Locations: 1
Eligibility criteria

Postmenopausal Female Patients with osteoporotic subcapital femoral neck fractur... [+1]

Patients that have undergone before osteoporotic fractures [+1]

Status: Recruiting

Virtual perI-/Menopause Registry of AusTrALia

13 million (50.7%) Australians are born with ovaries, 14% (\~3 million) are currently aged 40-59 yrs, \& all such who live to midlife will experience menopause, defined as \>12 months without a period. Peri-menopause (peri), typically occurs 5 yrs before menopause as hormone levels decrease. As with oestrogen, peri symptoms can affect every bodily system; e.g. depression/anxiety, diminished mental function, irregular periods, hot flushes, sleep problems, vaginal atrophy \& urinary urgency. These symptoms are linked with lower quality of life \& significantly higher work impairment; a third experiencing symptoms so severe as to impede daily life \& increase risk of suicide. Lifetime increased risks of diabetes, heart disease, osteoporosis \& dementia are also associated with menopause, yet it remains disconcertingly poorly studied. The investigators propose to create a world-first, cutting-edge, consumer-driven, Virtual peri-/menopause registry of AusTrALia (VITAL). The unique design will enable consumers to determine VITAL's questions, encourage secure revelation of private data e.g. vaginal \& mental health symptoms, \& to direct priorities for research, education, \& health service improvements. VITAL will thus deliver optimal assessments of incidence, prevalence \& impact. The participating consumers, researchers, clinical specialists, policy makers, \& modern virtual data infrastructure enable this unique \& innovative registry design, future translation to improved community health, \& promote awareness \& collaborative synergies. Leveraging the investigators' critical range of expertise \& ongoing feedback opportunities for both participants \& stakeholder partnerships, the investigators will create a ground-breaking platform that: * empowers the consumer voice and priorities, * enables peri-/menopause research to extend beyond existing niche focuses, * evidences the true impact of peri-/menopause across the nation, * evolves healthcare services and outcomes, \& * educates community, clinicians, \& policy-makers. After Australian registry establishment, the investigators will expand VITAL to mirror it in other nations while still protecting individual's data the right way, but so all can learn \& apply the best aspects of care from across the world.

Participants needed: 10,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Bespoke Clinical ResearchUpdated: Jul 5, 2024Locations: 1Duration: 50 Years
Eligibility criteria

Any Australian over 18 years of age.

None.

Status: Recruiting

Vascular Function, Sarcopenia and Pain in Postmenopausal Osteoporosis

This study aims to follow a cohort of osteoporotic patients treated with anti-osteoporotic drugs and to evaluate the impact of these treatments on the osteoporosis-cardiovascular-sarcopenia triad and on pain.

Participants needed: 150
Trial details
Age: 50+Biological sex: FemaleType: InterventionalSponsor: University Hospital, Clermont-FerrandUpdated: Oct 10, 2022Locations: 1
Eligibility criteria

Women aged 50 years or older with postmenopausal osteoporosis, whether fractured... [+2]

Patient with chronic renal failure, defined as glomerular filtration rate < 30 m... [+3]