Overview

This trial is active, not recruiting.

Condition hip fractures
Sponsor Active Implants
Start date April 2008
Trial size 11 participants
Trial identifier NCT00663468, TLV-0021-08

Summary

The purpose of this study is to determine the performance and efficacy during 6 and 12 month post operation.

1. determine changes in patient pain level

2. determine changes in patient functionality

3. determine changes in patient life quality

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Observational model case-only
Time perspective prospective
Arm

Eligibility Criteria

Male or female participants at least 60 years old.

Inclusion Criteria: - Female or male that is not younger than 60 years old. - Patient suffers from hip fracture that will need hip arthroplasty. - Patient that weight less than 150Kg - Patient femur head diameter between 40mm - 50mm - Mentally normal - Patient that could walk before suffering from hip fracture - Patient that willing to cooperate with the doctor - Patient that signed on the acceptance form Exclusion Criteria: - Patient that does not willing to cooperate with the doctor - Patient that is legally rejected - Patient that suffer from cancer - Patient that had passed amputation in is limbs - Patient that is paralysis - Patient that passed CVA or TIA - Patient that still recovering from hard wounds or surgery - Patient that suffer from infection in the hip joint

Trial information was received from ClinicalTrials.gov and was last updated in September 2012.
Information provided to ClinicalTrials.gov by Active Implants.