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Ultrasound Versus Fluoroscopic Guided Sacroiliac Joint Injection In Patients With Chronic Sacroiliac Joint Pain

Ultrasound Versus Fluoroscopic Guided Sacroiliac Joint Injection In Patients With Chronic Sacroiliac Joint Pain

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04446988
Enrollment
40
Registered
2020-06-25
Start date
2019-10-15
Completion date
2020-03-15
Last updated
2020-06-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sacro-Iliac Spondylosis

Keywords

Sacroiliac

Brief summary

Sacroiliac joint injection in sacroiliitis

Detailed description

Comparison of ultrasound guided and fluoroscopic guided sacroiliac joint injection

Interventions

Injection of sacroiliac joint with local anesthetic and steroid

Sponsors

Minia University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Sacroiliac joint injection with local anesthetic and steroid using ultrasound Versus fluoroscopy in sacroiliitis

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of sacroiliitis. * At least 3 positive physical examination maneuvers \[FABER (flexion, abduction, and external rotation), POSH (posterior shear), REAB (resisted abduction), Fortin's finger test\], * Moderate to severe pain (NRS pain score ≥ 3/10) refractory to oral anti-inflammatory. * Age from 18ys to 60ys.

Exclusion criteria

* Ages less than 18 or more than 85 years. * Body Mass Index (BMI) above 35 kg/m2. * A diagnosis of severe anxiety or depression and other psychological disorders. * Allergy to local anesthetics or steroids and pregnancy. * Multiple comorbidities (renal , hepatic, cardiac). * Coagulation disorder as bleeding tendency and platelet dysfunction. * Contraindication for prone position or radiological exposure. * Patient refuse . * Pain suggestive of bilateral sacroiliac joint involvement (it would have been difficult to assess pain and disability secondary to each SIJ).

Design outcomes

Primary

MeasureTime frameDescription
Numeric Rating Scale (NRS) pain scores3 monthsIt measures pain intensity (0 no pain - 10 worst pain imaginable)
Oswestry disability index score1 monthIt evaluates the physical function (0% minimal disability - 100% bed - bound patient)

Secondary

MeasureTime frameDescription
Analgesic requirement1 monthIt shows if the patient needs analgesic or not compared to pretreatment (type and dose in mg)
Patient satisfaction ( global perceived effect on a 7-point scale (GPE) )3 monthsIt shows if the patient satisfied with the procedure or not (1= worst ever - 7= best ever)
Procedure timeProcedureIt measures the seconds of procedure in both groups

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026