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NCT07105163Completed

Evaluation of Adherence With Bisphosphonates and Calcium and Vitamin D Supplements in Women With Postmenopausal Osteoporosis

Observational, Cross-sectional, Multicenter Study to Evaluate Adherence to Different Treatment Regimens With Oral Bisphosphonates and Calcium and Vitamin D Supplements in Postmenopausal Osteoporosis.

Source: ClinicalTrials.gov · Last updated 6 Oct 2026

Brief summary (registry, in English)

This study aims to evaluate the adherence of patients to combined treatment with bisphosphonates and calcium and vitamin D supplements, which is one of the usual treatments for postmenopausal osteoporosis. The study will consist of a single visit that will coincide with one of the patient's usual follow-up visits according to standard clinical practice. During this visit, information will be collected from the patient's medical history and an interview will be conducted using 3 questionnaires to assess how and how often the patient takes the treatment, possible forgetfulness, and whether or not the patient is satisfied with their current treatment.

Status (registry)
Completed
Study type
Observational
Enrollment
230 (actual)
First submitted
30 Jun 2025
Start date
3 Mar 2025
Primary completion date
3 Dec 2025
Lead sponsor
Procare Health Iberia S.L.
Diseases
Osteoporosis
NCT number
NCT07105163

What you commit to

  • Study type: Observational
  • Participants enrolled: 230
  • From 3 Mar 2025 to the primary completion date, 3 Dec 2025
  • 20 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • None

Who the study is looking for

  • \- Women diagnosed with postmenopausal OP.
  • \- Women who had been prescribed oral treatment with a BP administered monthly or weekly together with a Ca/D supplement (sachets or chewable tablets) administered daily, at least 6 months prior to inclusion in the study.
  • \- Women who had given their written informed consent before participating in the study.

Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (20)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
CP Dra Tejon
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AlicanteSpainUnknown status
CP Dra Medrano
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AlicanteSpainUnknown status
Hospital del Tajo
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AranjuezSpainUnknown status
CP Dra Sanchez
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BarcelonaSpainUnknown status
Hospital del Mar
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BarcelonaSpainUnknown status
Clinica Sagrada Familia
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BarcelonaSpainUnknown status
Hospital Reina Sofia
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CórdobaSpainUnknown status
CP Dr Caracuel
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CórdobaSpainUnknown status
CHU Insular - H Materno-Infantil
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Las Palmas de Gran CanariaSpainUnknown status
CP Dr Solano
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MadridSpainUnknown status
Hospital Infanta Leonor
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MadridSpainUnknown status
CP Dra Gerechter
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MadridSpainUnknown status
CP Dr Zafra
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MadridSpainUnknown status
Hospital Virgen del Mar
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MadridSpainUnknown status
CP Dr Agramonte
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Palma de MallorcaSpainUnknown status
CP Dr Balta
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Palma de MallorcaSpainUnknown status
Clínica Gaias - Santiago
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Santiago de CompostelaSpainUnknown status
Hospital Virgen Del Rocio
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SevilleSpainUnknown status
CP Dr Larrauri
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VigoSpainUnknown status
Hospital Zamora
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ZamoraSpainUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.