Actively Recruiting

Age: 55Years - 85Years
All Genders
Healthy Volunteers
NCT07228611

Assesment and Comparison of Osteoporosis Risk Factors After Stroke

Led by Ankara Etlik City Hospital · Updated on 2026-02-24

84

Participants Needed

1

Research Sites

21 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to evaluate the effect of these factors and stroke itself on osteoporosis developing after stroke. Thus, the expected benefit of the study is to contribute to the identification and determination of the need for treatment in high-risk patients through further studies. There are no expected risks from the study.

CONDITIONS

Official Title

Assesment and Comparison of Osteoporosis Risk Factors After Stroke

Who Can Participate

Age: 55Years - 85Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Followed by ischemic or hemorrhagic stroke
  • Between 1 week and 6 months or more than 1 year has passed since the date of the event
  • Being between 55 and 85 years of age
Not Eligible

You will not qualify if you...

  • The patient has additional neurological conditions besides stroke
  • The patient has a psychiatric condition
  • History of recurrent stroke
  • BMD scan performed within the last year for stroke patients
  • Having received osteoporosis treatment before or after the stroke
  • The patient having a fragility fracture before the stroke
  • The patient having a hip fracture or hip prosthesis
  • The patient having an additional condition that affects physical function before the stroke (amputation, severe fracture)
  • The patient has an additional disease or medication use that could cause secondary osteoporosis
  • The patient's stroke did not cause physical function loss

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

Ankara Etlik City Hospital

Ankara, Yenimahalle, Turkey (Türkiye), 06010

Actively Recruiting

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Research Team

A

Ayşe Naz Kalem Özgen, specialist

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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