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Sponsored by: |
Active Implants Israel Ltd. |
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Information provided by: | Active Implants Israel Ltd. |
ClinicalTrials.gov Identifier: | NCT00663468 |
The purpose of this study is to determine the performance and efficacy during 6 and 12 month post operation.
Condition |
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Hip Fractures |
Study Type: | Observational |
Study Design: | Case-Only, Prospective |
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Observation |
Ages Eligible for Study: | 60 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | Yes |
Sampling Method: | Non-Probability Sample |
community sample
Inclusion Criteria:
Exclusion Criteria:
Study ID Numbers: | TLV-0021-08 |
Study First Received: | April 17, 2008 |
Last Updated: | April 21, 2008 |
ClinicalTrials.gov Identifier: | NCT00663468 History of Changes |
Health Authority: | Israel: Ministry of Health |
determine changes in patient pain level determine changes in patient functionality determine changes in patient life quality |
Hip Fractures Femoral Fractures Fractures, Bone Wounds and Injuries |
Quality of Life Disorders of Environmental Origin Leg Injuries Pain |
Hip Fractures Femoral Fractures Fractures, Bone Wounds and Injuries |
Disorders of Environmental Origin Leg Injuries Hip Injuries |