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

M

Minia University

Status

Completed

Conditions

Sacro-Iliac Spondylosis

Treatments

Device: Sacroiliac joint injection

Study type

Interventional

Funder types

Other

Identifiers

NCT04446988
14102019

Details and patient eligibility

About

Sacroiliac joint injection in sacroiliitis

Full description

Comparison of ultrasound guided and fluoroscopic guided sacroiliac joint injection

Enrollment

40 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

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).

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

40 participants in 2 patient groups

Ultrasound(US)
Experimental group
Description:
Sacroiliac joint injection using ultrasound
Treatment:
Device: Sacroiliac joint injection
Fluoroscopy(FL)
Experimental group
Description:
Sacroiliac joint injection using fluoroscopy
Treatment:
Device: Sacroiliac joint injection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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