Analgesic Effect of Sacral Submultifidus Block as an Adjunct to Sacroiliac Joint Injection

NCT ID
NCT07814729
Registry status
Recruiting
Study type
Not specified in the registry data
Phase
Not applicable
Sponsor
Fayoum University Hospital

Overview

ClinicalTrials.gov lists this study as Recruiting.

Enrollment: 54 participants (Estimated).

What is being studied

No interventions are listed in the registry data.

Who may be eligible

Ages
Not specified in the registry data
Sex
Not specified in the registry data
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: 1-patients aged above 21 years, both genders diagnosed with chronic sacroiliac joint pain with a rating on the numeric pain rating scale (NPRS) of at least 5, without radiculopathy lasting 3 months or longer, and Positive SI provocative tests: usually \> 3 positive tests ... 2-Failure of conservative therapy .3-Radiological exclusion of lumbar pathology. 4- Diagnostic SIJ block producing ≥75% pain relief. Exclusion Criteria: * 1\. refusal to participate. 2. Allergy or contraindication to local anesthetics. 3. Coagulation disorders or ongoing anticoagulant therapy. 4. Infection at the block injection site. 5. Chronic opioid use or substance abuse. 6. Neurological or psychiatric disorders affecting pain assessment. 7. Pregnancy.

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: Egypt

Sample of listed locations

  • Fayoum university Hospitl — Al Fayyum, Egypt — Site recruitment status not specified in the registry data

Study details

Start date
September 1, 2026
Primary completion date
March 1, 2027
First posted
September 11, 2026

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07814729
Registry last updated
September 16, 2026
QualifiedStudies registry data refreshed
September 21, 2026

View NCT07814729 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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