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NCT02155595 · ClinicalTrials.gov registry record

Pathogenesis of Atypical Femur Fractures on Long Term Bisphosphonate Therapy

A clinical trial, sponsored by Henry Ford Health System.

Completed
Registry status
738
Enrollment target

NCT02155595: Completed study, sponsored by Henry Ford Health System.

NCT02155595 is a clinical trial that has completed, run by Henry Ford Health System. The registered enrollment target is 738 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02155595 has completed, sponsored by Henry Ford Health System.

COMPLETED
Registry status
738 participants
Enrollment target

Study Summary

The purpose of this protocol is to determine the risk of atypical femoral shaft (thigh bone) fractures after long term fracture prevention therapy with a class of drugs called "bisphosphonates", colloquially referred to as Alendronate, risedronate, Ibandronate, and Zoledronate. In addition, the study is designed to find out which patient is most likely to develop this potential life changing complication and why. Finally, the results of this study will help clinicians to better understand the reason and thus tailor patient specific treatments…i.e., "the right treatment for the right patient for right duration."

Primary Outcome

Determine the prevalence of PBD and/or Atypical Femoral Fractures (AFF) in patients with post-menopausal or glucocorticoid related osteoporosis, either treated with bisphosphonate (BP) for more than 2 years or never treated with a BP

Interventions

  • OTHER 500 without BP treatment
  • OTHER 500 with BP treatment

Trial Details

FieldValue
Enrollment Target 738 participants
Start Date 2014-05
Est. Completion 2018-08-31
Henry Ford Health System

234 total trials

What the finished NCT02155595 record still lists

NCT02155595 is an observational study that tracks outcomes without assigning an intervention. The registered 738 participants enrollment target is mid-sized for trials with a published cap.

The record links to 0 conditions, and to 2 interventions - of which 500 without BP treatment is the first listed.

NCT02155595 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02155595 about?

NCT02155595 is a clinical study titled "Pathogenesis of Atypical Femur Fractures on Long Term Bisphosphonate Therapy". The purpose of this protocol is to determine the risk of atypical femoral shaft (thigh bone) fractures after long term fracture prevention therapy with a class of drugs called "bisphosphonates", colloquially referred to as Alendronate, risedronate, Ibandronate, and Zoledronate. In addition, the stu...

What is the current status of trial NCT02155595?

This trial is currently completed. The enrollment target is 738 participants. The study started on 2014-05. Estimated completion is 2018-08-31.

What interventions are being tested in trial NCT02155595?

The interventions under investigation include: 500 without BP treatment (OTHER), 500 with BP treatment (OTHER).

Who is sponsoring clinical trial NCT02155595?

This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT02155595, the US trial registry maintained by the National Library of Medicine. NCT02155595 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.