Assesment and Comparison of Osteoporosis Risk Factors After Stroke

Recruiting now

Conditions studied: Stroke Osteoporosis

In brief

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.

Key facts

Study ID

NCT07228611

Run by

Ankara Etlik City Hospital

People needed

84

Starts

2025-12-05

Expected to finish

2026-05-01

Last updated by the study team

2026-02-24

Who can join

Age: 55 and older, up to 85. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• Followed by ischemic or hemorrhagic stroke
• Between 1 week and 6 months or >1 year has passed since the date of the event
• Being between 55 and 85 years of age

You may not qualify if…

• 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

Where it is running

• Ankara Etlik City Hospital — Ankara, Yenimahalle, Turkey (Türkiye) (enrolling)

Full record on ClinicalTrials.gov

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