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Diagnostic blockade of sacroiliac joint in patients with pseudoradicular low back pain.

Completed
Conditions
sacroiliac joint pain
Registration Number
NL-OMON19885
Lead Sponsor
Department of Anesthesiology, VU university medical center
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
63
Inclusion Criteria

1. Pseudoradicular character of pain;

2. Pain below L5;

Exclusion Criteria

1. Allergy to iodine, lidocaine or cortocosteroide;

2. Pregnancy;

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The effect of the diagnostic blockade is evaluated through a 10 items BOX-score (box 1 represents no pain, box 10 represents the worst imaginable pain). Patients will fill the BOX-score (diary) in at home 3 times a day, during at least 4 weeks after a blockade.
Secondary Outcome Measures
NameTimeMethod
With the Roland Disability questionnaire and Oswestry Low Back Pain Disability Index the limitation caused by low back pain will be assessed. Global health will be assessed using the short form (SF)-36 and COOP-Wonca questionnaire. Additionally the duration of a pain free period and daily pain medication use will be reviewed.
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