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NCT01839682 · ClinicalTrials.gov registry record
Evaluation of Outcomes of DFine StabiliT Kyphoplasty in Vertebral Compression Fractures Due to Osteoporosis
A clinical trial of Osteoporosis and Vertebral Fracture, sponsored by Cedars-Sinai Medical Center.
- Completed
- Registry status
- 23
- Enrollment target
- 1
- Study location
NCT01839682 is a study of Osteoporosis and Vertebral Fracture that has completed, run by Cedars-Sinai Medical Center. The registered enrollment target is 23 participants, below the 1,546-participant average among 84 other Osteoporosis trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state.
The verdict
NCT01839682, a study of Osteoporosis and Vertebral Fracture, has completed, sponsored by Cedars-Sinai Medical Center.
- COMPLETED
- Registry status
- 23 participants
- Enrollment target
- 1
- Study location
Study Summary
This post-market surveillance research project consists of data collection at specified time points using standard questionnaire instruments to compare pain level, mobility and function pre and post procedure using the D-Fine StabiliT® Vertebral Augmentation System and StabiliT® Bone Cement, an FDA approved product used in the standard treatment of vertebral compression fractures.
Conditions Studied
Study Locations (1)
California
- Cedars-Sinai Medical Center - Los Angeles
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 23 participants |
| Start Date | 2009-06 |
| Est. Completion | 2011-07 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01839682
The ClinicalTrials.gov registry entry for NCT01839682 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 23 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,546-participant average among 84 other Osteoporosis trials with a reported enrollment target (99% lower). The listed sponsor is Cedars-Sinai Medical Center, which has 339 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Osteoporosis appearing as the primary indexed condition, and to 0 interventions.
NCT01839682 reports 1 study location spanning 1 distinct geographic area - top geographies include California.
Frequently Asked Questions
What is clinical trial NCT01839682 about?
NCT01839682 is a clinical study titled "Evaluation of Outcomes of DFine StabiliT Kyphoplasty in Vertebral Compression Fractures Due to Osteoporosis". This post-market surveillance research project consists of data collection at specified time points using standard questionnaire instruments to compare pain level, mobility and function pre and post procedure using the D-Fine StabiliT® Vertebral Augmentation System and StabiliT® Bone Cement, an FDA ...
What is the current status of trial NCT01839682?
This trial is currently completed. The enrollment target is 23 participants. The study started on 2009-06. Estimated completion is 2011-07.
What conditions does trial NCT01839682 study?
This clinical trial studies the following conditions: Osteoporosis, Vertebral Fracture.
Who is sponsoring clinical trial NCT01839682?
This trial is sponsored by Cedars-Sinai Medical Center, which has 339 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01839682 being conducted?
This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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