Low Back Pain Clinical Trial
Official title:
Datos de la Historia clínica y Del Examen físico y neurológico Que Orientan al diagnóstico de Dolor Originario en la articulación sacroilíaca
NCT number | NCT04381208 |
Other study ID # | 19-04-2019 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | April 19, 2019 |
Est. completion date | May 1, 2024 |
Verified date | April 2023 |
Source | University of Valencia |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
There are many patients coming daily to our office with the complaint of chronic lumbosacral pain radiating or not to the legs that need a proper diagnosis before any treatment is decided. The diagnosis, based mostly on radiological exams, carries a risk of failure to diagnose the sacroiliac joint as the cause of the pain. The study proposes that a quick interrogatory followed by a physical exam with the adequate provocative testing can raise the suspicion of the diagnosis that the pain is originating from the sacroiliac joint. Thereafter, a diagnostic sacroiliac joint block can be performed. The study aims to correlate findings from patient history and physical examination with eventual diagnosis.
Status | Recruiting |
Enrollment | 140 |
Est. completion date | May 1, 2024 |
Est. primary completion date | December 31, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Patient being evaluated in clinic for chronic low back or buttocks pain with or without radiation to the legs Exclusion Criteria: - Patient has already undergone surgery for the condition of interest - Inflammatory condition - Active cancer |
Country | Name | City | State |
---|---|---|---|
Spain | Hospital General Universitario de Valencia | Valencia |
Lead Sponsor | Collaborator |
---|---|
University of Valencia | Hospital General Universitario de Valencia |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Final diagnosis | Number of participants diagnosed with each condition of interest | 1-2 months |
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