Clinical Trial Details
— Status: Active, not recruiting
Administrative data
NCT number |
NCT04957251 |
Other study ID # |
IRB 150819-1 |
Secondary ID |
|
Status |
Active, not recruiting |
Phase |
N/A
|
First received |
|
Last updated |
|
Start date |
September 28, 2015 |
Est. completion date |
October 1, 2024 |
Study information
Verified date |
August 2023 |
Source |
Mount Carmel Health System |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Interventional
|
Clinical Trial Summary
Randomized trial to evaluate the role of the anterior vs posterior approach regarding
hemiarthroplasty of the hip. The Investigators' hypothesis is that the muscle sparing
anterior approach may result in improved function in the short term, which may allow shorter
hospital stay and quicker return to prior level of function.
Description:
Background
In patients who sustain a displaced femoral neck fracture, who do not meet criteria for total
hip arthroplasty, the recommendations are made for a hemi-arthroplasty of the hip. There are
multiple surgical approaches that can be used including the anterior approach to the hip and
the posterior approach to the hip. The most widely performed approach to the hip when
performing a total hip arthroplasty or hemi-arthroplasty has been the posterior approach.
However, multiple approaches exist including posterior approach, direct lateral approach,
anterolateral approach and direct anterior approach. There is not a consensus about which
approach is the most appropriate or best for patients. The decision for approach is widely
decided by the surgeon and is based on experience and preference of the surgeon. Recent
advances in the anterior approach to the hip have found improved results with regards to
functional status and decreased complications when compared to the posterior approach for
total hip arthroplasty. There have been several retrospective studies comparing the anterior
vs. posterior approach for hemi-arthroplasty with regards to treatment of femoral neck
fractures. These studies have shown conflicting results with regards to which approach is
superior. Retrospective studies have shown decreased dislocation rate with the anterior
approach, but increased operative time and increased rate of infection with anterior approach
as well. To date, there have been two prospective studies performed comparing the anterior
and posterior approach for hemi-arthroplasty, one in Japan and one in France, both of which
showed decreased dislocation rates but did not display long term functional improvement
comparing the two approaches. Both of these studies' patient population and protocol differ
greatly from standard of care in the United States. To date, there have been no prospective
randomized controlled trials evaluating the functional advantage of the anterior vs. the
posterior approach when performing hip hemi-arthroplasty procedure for femoral neck fractures
in the United States. It is our hypothesis that the anterior approach will provide superior
functional results as a product of the decreased damage to soft tissue and restoration of
normal anatomy.
Objectives:
There are several objectives of this study.
The main objective of this study is to evaluate the functional status of each patient using a
Harris Hip Score to evaluate both function and pain comparing the anterior vs. the posterior
approach for hemi-arthroplasty at 6 months.
Secondary objectives of this study include:
- time to ambulation post operatively
- rate of complications including infection, nerve palsy, and DVT/PE
- operative time
- rate of dislocation
- periprosthetic fracture
- mortality
- return to preoperative mobility status
- blood loss
Significance:
The results of this study would either confirm the retrospective data that currently exists
showing no difference in functional outcomes between the two approaches or demonstrate a
superior functional status with either the anterior or posterior approach for hip
hemi-arthroplasty. Of which, logically and anecdotally, the Investigators' believe will be
the anterior approach. With this research, theInvestigators' believe the anterior approach
can become the standard of care for the surgical technique with regards to hemi-arthroplasty
for hip fractures
Eligible patients:
Eligible patients will include all patients that were previously ambulatory at some level who
sustain a displaced femoral neck fracture that given functional status, age, and
comorbidities will require a hemi-arthroplasty for definitive treatment. Ages 65-99
Patients who will be excluded from the study are all patients who are non ambulatory at
baseline.
Design:
Patients who meet eligibility criteria will be offered to participate in the study. Once the
patient consents, the participants will be randomized to receive either the anterior or
posterior approach for hemi-arthroplasty of the hip. After surgery, the participant will
undergo standard postoperative care (hip precautions) with data collected from the electronic
health record and from standard hospital care including rounding. The participant will then
follow up at appropriate standard interval with the main endpoint of 6 months where Harris
Hip Scores will be used to judge the participant's functional status as well as pain relief.
Analysis of the collected data will occur at intervals of 50 patients to evaluate trends or
statistical significance.
Monitoring Participants:
If at any time during this study the participant or medical decision maker decides to no
longer participate in the study, the participant will be removed from the study and will
continue to undergo standard treatment for their condition.
Consent:
Consent will be obtained so long as the participant meets the appropriate criteria listed
above and will be given a detailed informed consent document outlining the purpose of the
study and associated risks and benefits.
Human Subject Protections:
There is currently no widely accepted technique based on outcomes with regards to operative
approach for hip hemi-arthroplasty, nor is there a standard approach for total hip
arthroplasty. Therefore, the participant will not have to do anything different from an
intervention standpoint and therefore are not at any increased risk based on our study
protocol. All participants will receive treatment of hip fracture in an appropriate fashion.
They will be asked standard postoperative questions during their stay and will undergo
standard follow up. The only change from current standard of care in follow up will include
the primary investigator performing a Harris Hip questionnaire and assessment at each
postoperative visit.
With regards to selection, the only criteria will be a baseline ambulatory status prior to
sustaining a displaced femoral neck fracture. The participants who are demented will be
included in the study because a large percentage of patients who sustain femoral neck
fractures and require a hemi-arthroplasty have some baseline dementia. These participants
will only be included if a medical power of attorney or appropriate medical decision maker is
available.
Analysis
Data will be collected and analyzed after 50 participants using a student t-test analysis to
evaluate for statistical significance or tends. The goal of 200 patients is to obtain the
largest prospective controlled trial to date. Analysis every 50 is based off of previous
literature that showed statistical significance near 50 patients in some categories including
dislocation.
Adverse Events Reporting
This study is a single surgeon study that is not blinded and all adverse events outside of
the expected complications associated with hip hemi-arthroplasty will be reported immediately
to the IRB board.
Patient confidentiality
The only PHI data that will be kept will be the FIN number to pull information from the
electronic health record during analysis. This is necessary as a means to be able to
accurately report lab values, operative times, and other pertinent information from their
hospital stay. Otherwise, all hard copy data will be locked in a safe location, and all
electronic data will be password protected.