Back Pain Clinical Trial
Official title:
IRB-HSR # 14073 Investigation of Pelvic Girdle Dysfunction in the Low Back Pain Population
The subjects will undergo a specific physical exam of tests reported to be diagnostic of
sacroiliac joint (SIJ) pain prior to receiving the routine injection in the SIJ that which
is being performed as part of their normal medical care. Routine care involves use of any
number of these tests, but doesn't routinely include assessment of all 6 tests in all
patient's treatment. The subject will fill out a Visual Analog Scale for pain and a pain
drawing prior to and after the injection.
The tests will be repeated after the injection.
The investigators propose to investigate a cluster of tests proposed by Laslett as well as
compare the results of the ASLR and the Gillet Test both before and after SIJ injection to
determine the validity of these tests in a low back patients presenting for injections
thought to be from the sacroiliac joint. The secondary purpose would be the development of a
clinical predictor rule to determine examination characteristics of patients who may benefit
from intraarticular injections of the SIJ.
Low back pain has been the subject of extensive research in the past 10 years. Some of the
efforts have focused on the effectiveness of diagnostic testing in determining the etiology
of low back pain. One component of low back pain clinically can be sacroiliac joint (SIJ)
dysfunction. The prevalence of sacroiliac pain in the low back pain population is reported
to be approximately 10 to 30%. The diagnosis of sacroiliac pain has been an area of
controversy in the literature with poor inter-tester and intra-rater reliability described
for motion testing. More recently, a cluster of provocation tests has been described as
predictive of the diagnosis of sacroiliac dysfunction. Laslett et al suggested that SI pain
provocation tests used in examination should include a cluster of six tests. When three or
more out of six tests or any two of four selected tests are positive, that showed the best
predictive power in diagnosing SIJ pain. The "gold standard" for diagnosing SIJ pain in this
study was pain relief with intra-articular local anesthetic block injection. When all six
provocation tests do not provoke the patient's typical pain, the SIJ can be ruled out as a
source of current low back pain.
Pelvic girdle pain including SIJ dysfunction has been investigated in post partum
populations. The Active Straight Leg Raise (ASLR) has been shown to be reliable in post
partum pelvic pain. This test is thought to help assess hypermobility in the SIJ. This test
has a positive likelihood ratio (+LR)= 14.5 and a negative likelihood ratio (-LR)= .14 which
indicates that this is a good test to rule in or rule out pelvic girdle pain in pregnancy.
This test is thought to help assess dysfunction of the SIJ. The Gillet test has recently
been reported to indicate abnormal biomechanics on the stance side by Hungerford et al.
Increased hamstring activation on the stance leg has been identified as indicative of
abnormal SI motion. These two tests (ASLR and Gillet) are thought to be reflective of SIJ
instability or abnormal movement in, respectively, pregnancy or low back patients.
;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Health Services Research
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT05982483 -
Erector Spinae Plane Block vs. Usual Care for ED Patients With Mechanical Back Pain
|
N/A | |
Completed |
NCT04744246 -
Muscle Activity During Load Carriage in ROTC Cadets
|
N/A | |
Completed |
NCT03273114 -
Cognitive Functional Therapy (CFT) Compared With Core Training Exercise and Manual Therapy (CORE-MT) in Patients With Chronic Low Back Pain
|
N/A | |
Active, not recruiting |
NCT03680846 -
Comparison of HF10 Therapy Combined With CMM to CMM Alone in the Treatment of Non-Surgical Refractory Back Pain
|
N/A | |
Completed |
NCT05597189 -
Clinical Study for Palliative/Preventive Treatment of Chronic Back Pain
|
N/A | |
Completed |
NCT05342181 -
Static and Dynamic Core Stability Exercises in Potpartum Back Pain
|
N/A | |
Completed |
NCT02955342 -
Back and Neck Pain in Adolescence
|
||
Not yet recruiting |
NCT02536274 -
"Examination of the Impact of a Dynamic Flexion Orthosis (Dynaflex®Ottobock) or of a Back Bandage (Lumbo Sensa®Ottobock) on the Voluntary Activation of the Back Muscles in Patients With Specific Back Pain"
|
N/A | |
Completed |
NCT02704845 -
Biopsychosocial Exploration of Pain Profiles in Inflammatory and Chronic Non-specific Axial Low Back Pain
|
N/A | |
Recruiting |
NCT02237105 -
The Effect of Cognitive Behavioral Therapy on the Outcome of Spinal Surgery
|
N/A | |
Enrolling by invitation |
NCT02485795 -
Observational Study of the Impact of Genetic Testing on Healthcare Decisions and Care in Interventional Pain Management
|
N/A | |
Completed |
NCT02254694 -
The Influence of High Heeled Shoes on the Sagittal Balance of the Spine and Whole Body
|
N/A | |
Completed |
NCT02609009 -
Back Pain and Spinal Manipulation in Adolescent Scoliosis
|
N/A | |
Terminated |
NCT02239627 -
Epidural Clonidine Versus Corticosteroid for Low Back Pain
|
N/A | |
Completed |
NCT00986180 -
NUCYNTA (Tapentadol Immediate Release) Versus Oxycodone Immediate Release in the Treatment of Acute Low Back Pain
|
Phase 3 | |
Terminated |
NCT00769626 -
Standardizing Management of Patients With Low Back Pain in Primary Care and Physical Therapy
|
Phase 3 | |
Completed |
NCT00771758 -
Tapentadol IR vs Oxycodone IR vs Placebo in Acute Pain From Vertebral Compression Fracture Associated With Osteoporosis
|
Phase 3 | |
Withdrawn |
NCT00231374 -
Measure of Cerebrospinal Fluid (CSF) Pressure Variation With Patient Positioning
|
N/A | |
Completed |
NCT00454064 -
Cognitive-behavioural Treatment of Chronic Back Pain
|
Phase 3 | |
Completed |
NCT00103675 -
Sensor Measurement of Acupuncture Needle Manipulation
|
Phase 1 |