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OpenTrials
Completed

NCT Number: NCT00166374

To Evaluate Success of Cement Treatment of Spinal Compression Fractures

Patients with vertebral compression fracture will be treated cement injection into the spine and monitored using standard evaluations.

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Key information

Conditions

Back Pain Neurologic Manifestations Pain Pathological Conditions, Signs and Symptoms Signs and Symptoms

Age range

20 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mayo Clinic

Rochester, Minnesota, 55905, United States

About this study

Patients with vertebral compression fracture will be diagnosed and treated with balloon kyphoplasty. Pain and functional status will be assessed at baseline, 1-, 12-, and 24-months post-operatively using VAS pain scale, Oswestry Disability Index, and SF-36.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

vertebral compression fracture

Treatment and study plan

balloon kyphoplasty

Procedure

Primary outcomes

  1. pain

  2. disability

Sponsors and collaborators

Lead sponsor

Mayo Clinic

Other

Registry information

Official study title

Outcomes Following Balloon Kyphoplasty for Vertebral Compression Fracture

Important dates

Primary completion
2007
Study completion
2007
First posted
Sep 14, 2005
Registry last updated
Jan 20, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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