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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT02260726
Other study ID # 20140318-01H
Secondary ID
Status Withdrawn
Phase N/A
First received October 6, 2014
Last updated April 13, 2018
Start date October 2014
Est. completion date October 2016

Study information

Verified date April 2018
Source Ottawa Hospital Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients are being asked to participate in this study because a previous research MRI of their hips showed that the shape of the head of their thigh bone may indicate FAI of the hip. We have already collected cartilage imaging data and data on how the hip joint moves on people with painful/symptomatic FAI and people with normal hip function. We would now like to compare the motion of the hip joint to those with painful FAI using ultrasound.


Description:

Hip impingement is thought to be a leading cause of hip osteoarthritis, and occurs due to deformities in the hip joint. However some individuals have these deformities but do not exhibit symptoms. Using the standard magnetic resonance imaging and clinical tests it is not clear which deformities will cause degeneration, requiring surgical intervention. We propose to evaluate the deformity and impingement between the femur and acetabulum using dynamic ultrasound imaging. Ultrasound does not involve radiation and can acquire video of the hip joint and is thus suitable for such diagnostic purposes. In this pilot study we will evaluate the feasibility of ultrasound in diagnosing hip impingement.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date October 2016
Est. primary completion date October 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

Surgical group:

- Hip pain longer than 6 months referred to the groin/lateral aspect of the hip

- Positive Impingement Sign

Plain radiographs:

- Absence of arthritis (Tonnis Grade 0 or 1)

- Absence of dysplasia (center edge >25 degrees) on anterior-posterior radiograph

- a-angle greater than 60 degrees on MRI.

Exclusion Criteria:

- Patients who don't meet inclusion criteria

- Control group: subjects with hip pain or with alpha angle > 50 degrees on MRI

Study Design


Intervention

Procedure:
Magnetic resonance imaging

Ultrasound


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Ottawa Hospital Research Institute

Outcome

Type Measure Description Time frame Safety issue
Primary Ultrasound grade Ultrasound grade evaluated on a four point scale following ultrasound imaging session Upon enrollment
Secondary Ultrasound parameters Morphometry of hip measured in ultrasound images: alpha angle, clearance angle Upon enrollment
Secondary MRI parameters Standard MRI measures of impingement from images. Used as gold standard for comparative purposes. Upon enrollment
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