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Long Term Follow-Up After Patients Underwent Total Hip Replacement

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ClinicalTrials.gov Identifier: NCT01687322
Recruitment Status : Unknown
Verified March 2013 by iri liebergall, Hadassah Medical Organization.
Recruitment status was:  Active, not recruiting
First Posted : September 18, 2012
Last Update Posted : March 20, 2013
Sponsor:
Information provided by (Responsible Party):
iri liebergall, Hadassah Medical Organization

Brief Summary:
The investigators want to contact patients that underwent total hip replacement for the past ten years. The investigators will ask them about their daily living, functioning and quality of life.

Condition or disease
Total Hip Replacement Pain

Study Type : Observational
Estimated Enrollment : 150 participants
Time Perspective: Prospective
Study Start Date : January 2013
Estimated Primary Completion Date : January 2015

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Hip Replacement
U.S. FDA Resources

Group/Cohort
total hip replacement, quality of life, functioning



Primary Outcome Measures :
  1. quality of life [ Time Frame: up to ten years ]
    quality of life will be assessed by the SF-12 questionnaire. We will compare between the results from the last visit to the current.


Secondary Outcome Measures :
  1. functioning [ Time Frame: up to ten years ]
    functioning will be assessed by the Harris Hip Score. We will compare between the results from the last visit to the current visit



Information from the National Library of Medicine

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Ages Eligible for Study:   28 Years to 85 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
men and women than underwent total hup replacment
Criteria

Inclusion Criteria:

1. total hip replacement from 01.01.2002

Exclusion Criteria:

1. no


Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01687322


Locations
Israel
Hadassah Medical Organization
Jerusalem, Israel
Sponsors and Collaborators
Hadassah Medical Organization

Responsible Party: iri liebergall, Prof Meir (Iri) Liebergall, Chairman, Orthopedic Surgery Dept., Hadassah Medical Organization
ClinicalTrials.gov Identifier: NCT01687322     History of Changes
Other Study ID Numbers: lieb004-CTIL-HMO
First Posted: September 18, 2012    Key Record Dates
Last Update Posted: March 20, 2013
Last Verified: March 2013

Keywords provided by iri liebergall, Hadassah Medical Organization:
quality of life
functioning