Actively Recruiting
Effect of Probiotics After Neurosurgery
Led by University Maribor · Updated on 2025-11-28
110
Participants Needed
1
Research Sites
82 weeks
Total Duration
On this page
Sponsors
U
University Maribor
Lead Sponsor
U
University Medical Centre Maribor
Collaborating Sponsor
AI-Summary
What this Trial Is About
The goal of this randomised controlled trial is to determine the effect of consuming a multistrain probiotic OMNi-BiOTiC® Hetox on improving the healing, pain management, and postsurgical complications after neurosurgery. The main question it aims to answer is: • Is the multistrain probiotic OMNi-BiOTiC® Hetox effective in in improving patient-reported disability after neurosurgery? Researchers will compare the probiotic group and the placebo group to determine if the healing is significantly different between the groups.
CONDITIONS
Official Title
Effect of Probiotics After Neurosurgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults with MRI-confirmed disc herniation, stenosis, or instability of the lumbar or cervical spine
- Able to provide written informed consent
- Willing to comply with study procedures and follow-up assessments
- No contraindications to probiotic administration
You will not qualify if you...
- Symptoms of acute infection such as vomiting, fever above 386C, diarrhea, or respiratory symptoms
- Presence of chronic diseases
- Use of probiotics within one month before inclusion
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University Medical Centre Maribor
Maribor, Slovenia
Actively Recruiting
Research Team
S
SABINA FIJAN, Ph.D.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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