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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT00756431
Other study ID # BMET UK 06
Secondary ID
Status Withdrawn
Phase N/A
First received September 19, 2008
Last updated June 16, 2017
Start date January 2004
Est. completion date June 2010

Study information

Verified date June 2017
Source Zimmer Biomet
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Evaluated whether HA coated dynamic hip screws can improve the surgical results in trochanteric femoral fractures


Description:

Randomised study to determine the effect of HA coating on the stability of lag screws used to reduce femoral neck fractures. Stability of the screw will be determined by RSA measurements. The effect of the HA coating on bone remodeling will be determined by DEXA measurements


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date June 2010
Est. primary completion date June 2010
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients with trochanteric femoral fractures

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Hip Fracture reduction Screw without HA Coating (Hiploc)
Hip Fracture reduction Screw without HA Coating (Hiploc)
Hip Fracture reduction Screw with HA Coating (Hiploc)
Hip Fracture reduction Screw with HA Coating (Hiploc)

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
Zimmer Biomet Biomet U.K. Ltd., Hvidovre University Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary Harris Hip Score 3months, 6 months
Secondary DEXA 3months, 6 months
Secondary RSA 3months,6 months
Secondary Complications Anytime
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