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

NCT ID: NCT04446988

Last Updated: 2020-06-25

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-10-15

Study Completion Date

2020-03-15

Brief Summary

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Sacroiliac joint injection in sacroiliitis

Detailed Description

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Comparison of ultrasound guided and fluoroscopic guided sacroiliac joint injection

Conditions

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Sacro-Iliac Spondylosis

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

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

TREATMENT

Blinding Strategy

NONE

Study Groups

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Ultrasound(US)

Sacroiliac joint injection using ultrasound

Group Type EXPERIMENTAL

Sacroiliac joint injection

Intervention Type DEVICE

Injection of sacroiliac joint with local anesthetic and steroid

Fluoroscopy(FL)

Sacroiliac joint injection using fluoroscopy

Group Type EXPERIMENTAL

Sacroiliac joint injection

Intervention Type DEVICE

Injection of sacroiliac joint with local anesthetic and steroid

Interventions

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Sacroiliac joint injection

Injection of sacroiliac joint with local anesthetic and steroid

Intervention Type DEVICE

Eligibility Criteria

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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).
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Minia University

OTHER

Sponsor Role lead

Responsible Party

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DR. Abd El-Raheem Mahmoud

Clinical Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Hany Ka Mickhael, Ass. pr.

Role: PRINCIPAL_INVESTIGATOR

Minia University

Locations

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ASSIUT University Hospitals

Asyut, , Egypt

Site Status

Countries

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Egypt

References

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Benson DA, Cavanaugh M, Clark K, Karsch-Mizrachi I, Lipman DJ, Ostell J, Sayers EW. GenBank. Nucleic Acids Res. 2013 Jan;41(Database issue):D36-42. doi: 10.1093/nar/gks1195. Epub 2012 Nov 27.

Reference Type RESULT
PMID: 23193287 (View on PubMed)

Other Identifiers

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14102019

Identifier Type: -

Identifier Source: org_study_id

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