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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05090553
Other study ID # VMRDocProtocol_2021
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date August 1, 2021
Est. completion date October 1, 2022

Study information

Verified date August 2022
Source Gaffree & Guinle Universitary Hospital
Contact Vinicius M da Rocha, MD
Phone 55 21 99700-7240
Email viniciusmagnodarocha@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study aims to identify metabolites present in intervertebral discs colonized by C. acnes from patients with low back pain and degenerative disc disease, correlating them with their clinical, radiological and demographic profiles.


Recruitment information / eligibility

Status Recruiting
Enrollment 120
Est. completion date October 1, 2022
Est. primary completion date August 1, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: - low back pain lasting longer than 3 months; - MRI findings of degenerative lumbar discopathy (DDL) performed less than 6 months after inclusion in the study; - indication for open surgical treatment, with isolated microdiscectomy or associated with lumbar arthrodesis; - failure of conservative treatment for at least 6 weeks and/or progressive neurological deficit Exclusion Criteria: - History of open lumbar spine surgery at any stage of life; - presence of chemotherapy or pulse therapy with corticoids; - patients with immune deficiency; - patients undergoing previous intradiscal therapies (nucleotomy or discography); - patients undergoing previous endoscopic surgery; - patients with a history of previous spinal infection treated with antibiotics in the 6 months prior to inclusion in the study; - use of antibiotics in the 2 months prior to the surgical procedure

Study Design


Intervention

Procedure:
Lumbar Spinal Fusion Surgery
During surgery will be collected five disc fragments and five fragments of muscle-ligament tissue adjacent to the collected disc.
Biological:
Bacterial culture
Samples will be seeded on blood agar and anaerobic blood agar plates. After sowing in solid media, the swab will be inoculated in thioglycolate medium, where it will remain for 14 days
Genetic:
Phenotypic and genotypic characterization
The phenotypic identification of the species will be carried out through mass spectrometry, with the MALDI-TOF equipment. PCR analyzes performed in two phases, the first to confirm the presence of bacteria (target and non-target) using primers capable of amplifying eubacteria ribosomal deoxyribonucleic acid (rDNA) 16s and the second directed to confirm C. acnes through specific rDNA 16s primers.
Multiomics analysis
Whole Genome Sequencing, proteomics and metabolomics analysis

Locations

Country Name City State
Brazil Hospital Universitário Gaffrée e Guinle Rio de Janeiro

Sponsors (3)

Lead Sponsor Collaborator
Gaffree & Guinle Universitary Hospital Conselho Nacional de Desenvolvimento Científico e Tecnológico, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.

Country where clinical trial is conducted

Brazil, 

Outcome

Type Measure Description Time frame Safety issue
Primary Incidence of C. acnes on intervertebral disc Incidence of C. acnes on intervertebral disc in patients with chronic low back pain and DDL. Up to 5 months
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