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
• Status: Not yet recruiting
• 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
• 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

Related Conditions & MeSH terms

• Patient Compliance
• Patient Satisfaction

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