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NCT04243980 Clinical Trial

Anatomical Femoral Stem in Total Hip Arthroplasty

Patient Satisfaction Clinical Trial

— THR  

Official title:
Short Term Results of Short Anatomical Femoral Stem in Total Hip Arthroplasty - Prospective Study

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT04243980
Other study ID # EMC-19-0100
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date February 1, 2020
Est. completion date January 1, 2022

Study information
Verified date January 2020
Source HaEmek Medical Center, Israel
Contact Raja Hakim, M.D.
Phone 00972546612251
Email raja.hakim@icloud.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

A study that detect the femoral anteversion after total hip arthroplasty using short anatomical femoral stem compared to the contrast side

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 50
Est. completion date January 1, 2022
Est. primary completion date January 1, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- age 18-90

- patients who had THR as an elective surgery

- patients who had THR with short femoral anatomical stem

Exclusion Criteria:

- severe osteoporosis with Dorr C classification

- s/p bilateral hip arthroplasty

- non-complaint patients

- revision surgery

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Short anatomical femoral stem in THR
Patients with osteoarthritis after total hip arthroplasty

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
HaEmek Medical Center, Israel

Outcome
Type Measure Description Time frame Safety issue
Primary Femoral anteversion comparing femoral anteversion after THR using CT scan Post-Operatively, through study completion, an average of 2 years
Secondary Harris Hip Score The HHS is a physician-completed instrument that consists of subscales for pain severity (1 item, 0-44 points), function (7 items, 0-47 points), absence of deformity (1 item, 0-4 points), and range of motion (2 items, 0-5 points).
Where a score < 70 indicating a poor result and those of 90-100 indicating an excellent result		 6 weeks, 3 month, 6 month post-operative
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