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NCT07112677

Seroprevalence of Brucella Antibodies in High-Risk Patients With Low Back Pain: A Case-Control Study

Completed Last updated 8 August 2025
What this trial tests

trial testing Brucella Antibody Testing (ELISA) in Brucellosis in 100 participants. Completed in 28 February 2025.

Timeline
1 February 2024
Primary endpoint
28 February 2025
28 February 2025

Quick facts

Lead sponsorElham Ahmed Hassan
StatusCompleted
Study typeOBSERVATIONAL
Enrollment100
Start date1 February 2024
Primary completion28 February 2025
Estimated completion28 February 2025
Sites2 locations across Egypt

Drugs / interventions tested

Conditions studied

Sponsor

Elham Ahmed Hassan

Who can join

18 and older, any sex, with Brucellosis or Low Back Pain. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this observational case-control study is to assess the presence of Brucella antibodies in patients with low back pain who are at high risk for brucellosis exposure, such as those with animal contact or consumption of unpasteurized dairy products. The main question it aims to answer is: Is there a significant association between Brucella seropositivity and low back pain in high-risk individuals? Researchers will compare patients with low back pain to age- and sex-matched healthy controls without back pain but with similar exposure risks, to see if Brucella antibodies are more frequent in the patient group. Participants will: Undergo a detailed clinical history and physical examination Provide blood samples for serological testing using ELISA for Brucella IgG/IgM/IgA Be evaluated for other symptoms such as fever, fatigue, and joint pain

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Brucellosis

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07112677.

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