Osteoporosis Trial, Recruiting NCT07253493 Sponsor: Istanbul Physical Medicine Rehabilitation Training and Research Hospital Condition: Osteoporosis
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Osteoporosis Trial, Recruiting

NCT07253493
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You must be postmenopausal (your periods have permanently stopped).
  • For the osteoporosis group: you must have been diagnosed with osteoporosis in the hip area, shown by specific bone density scan scores at the femoral neck or total hip (T-score of -2.5 or lower).
  • For the control group (no bone disease): your bone density scan scores must be in the normal range at the hip and lower spine (T-score above -1 in all measured areas).
  • You must be willing to participate voluntarily.

Who may not be able to join:

  • You are currently receiving any treatment for osteoporosis.
  • You have a condition affecting your nervous system, such as a history of stroke, nerve damage, or nerve compression (confirm with trial site).
  • You have any muscle disease, whether inherited or developed over time.
  • You have active pain in your legs or lower joints, such as osteoarthritis or inflammatory joint conditions.
  • You have an irregular heartbeat (cardiac arrhythmia).
  • You have a history of any other disease that affects bone metabolism (confirm with trial site).
  • You have any skin sores, wounds, or lesions on your lower legs or feet where sensor pads (electrodes) would need to be placed.
  • You are older than 65 years of age.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: İlhan Karacan, Prof. Dr., stanbul Physical Medicine Rehabilitation Training and Research Hospital

Phone: +905348431984

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Istanbul Physical Medicine Rehabilitation Training and Research Hospital
Registry
ClinicalTrials.gov
Start date
18 November 2025
Est. completion
1 March 2026

Where this trial is recruiting

Turkey (Türkiye)

Primary endpoints

H-reflex Amplitude

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov