Hip Dysplasia Clinical Trial
Official title:
Stress Analysis of Hip Dysplasia After Corrective Surgery
NCT number | NCT01575977 |
Other study ID # | 43600 |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | February 2011 |
Est. completion date | August 2019 |
Verified date | October 2019 |
Source | University of Utah |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The main objective of this study is to predict cartilage contact pressures in the hip after periacetabular osteotomy (PAO).
Status | Completed |
Enrollment | 12 |
Est. completion date | August 2019 |
Est. primary completion date | August 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 40 Years |
Eligibility |
Inclusion Criteria: - Patients aged 18-40 years - Patients who have undergone periacetabular osteotomy by Dr. Peters for treatment of hip dysplasia. - Patients who have previously participated in IRB #10983 "Comparative Stress Analysis of Hip Dysplasia". Exclusion Criteria: - Persons with a history of allergies to lidocaine or seafood. - Children under the age of 18. - Persons incarcerated, on trial, or parole. - Women who are pregnant. - Subjects who do not have high quality pre-operative images available or have not been surgically treated by periacetabular osteotomy. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
University of Utah |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | To predict cartilage contact pressures in the hip joint during simulated daily activities before and after periacetabular osteotomy (PAO) for correction of traditional dysplasia/retroversion. | 1 year post surgery |
Status | Clinical Trial | Phase | |
---|---|---|---|
Enrolling by invitation |
NCT05543109 -
Ultrasound Guided Psoas Compartment Block vs Suprainguinal Fascia Iliaca Compartment Block
|
N/A | |
Active, not recruiting |
NCT03326804 -
H1 Hip Resurfacing Arthroplasty
|
||
Active, not recruiting |
NCT05142462 -
Post Market Clinical Follow-up of EUROSCUP Fixe Acetabular Cup
|
||
Recruiting |
NCT03109444 -
Normative Radiographic Parameters and Growth Curve of Hips Less Than Six Weeks of Gestational Age Using Ultrasound
|
||
Withdrawn |
NCT02259140 -
A Randomized Control Trial of Hip Dislocation Techniques for Pediatric Patients With Cerebral Palsy
|
N/A | |
Completed |
NCT06087549 -
PENG Block vs. ESP Block for Pediatric Hip Surgery
|
Phase 4 | |
Completed |
NCT03874936 -
The Effect of Perioperative Dexamethasone Administration on Postoperative Pain in Patients Undergoing Periacetabular Osteotomy.
|
Phase 2/Phase 3 | |
Active, not recruiting |
NCT04943328 -
Cemented TrendHip® - Multicenter PMCF Study on Total Indications
|
N/A | |
Not yet recruiting |
NCT04157842 -
The Influence of Hip Replacement on Lower Extremity Hemodynamics in Crowe IV Hip Dysplasia Patient
|
N/A | |
Active, not recruiting |
NCT04995822 -
Post Market Clinical Follow-up of EUROSTEM Femoral Stem
|
||
Recruiting |
NCT05687955 -
Exercise Rehabilitation for Hip-related Pain and Dysfunction in Student Circus Arts Performers
|
N/A | |
Completed |
NCT01344421 -
Movement Pattern in Patients With Hip Dysplasia
|
N/A | |
Recruiting |
NCT05366712 -
Nexus Evaluation Primary Trident II Uncemented Shell
|
N/A | |
Recruiting |
NCT04993638 -
Post Market Clinical Follow-up of Dual-mobility Acetabular Cup EUROSCUP MOBILE
|
||
Completed |
NCT04591067 -
Physical Capacity Among Patients Treated With Periacetabular Osteotomy for Hip Dysplasia: a Cross-sectional Study
|
||
Withdrawn |
NCT03530878 -
Mild Hip Dysplasia
|
N/A | |
Not yet recruiting |
NCT03193385 -
Treatment of Developmental Dysplasia of the HIp
|
N/A | |
Not yet recruiting |
NCT05921721 -
Can EOS Hip Imaging Replace CT Hip Scans?
|
N/A | |
Active, not recruiting |
NCT03941171 -
Is Periacetabular Osteotomy Superior to Progressive Resistance Training?
|
N/A | |
Recruiting |
NCT05361980 -
Pediatric Orthopaedic Implant Safety & Efficacy
|