Actively Recruiting
Probiotics for Improving Post-surgical Healing
Led by University of Pisa · Updated on 2024-05-09
150
Participants Needed
1
Research Sites
189 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
A randomized, double-blind, placebo-controlled clinical trial will be performed to assess the efficacy of a probiotic containing Lactobacillus reuteri in improving post-surgical wound healing after impacted tooth extractions. The Primary aim is to evaluate the efficacy of L. reuteri in improving post-extractive healing. The Secondary aim is to evaluate the efficacy of L. reuteri in association with an antibiotic therapy (amoxicillin) in reducing the incidence and severity of antibiotic-associated gastro-intestinal symptoms.
CONDITIONS
Official Title
Probiotics for Improving Post-surgical Healing
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Need for impacted tooth extractions
- Age 18 years or older
- Ability to understand and sign an informed consent form
You will not qualify if you...
- Allergy to penicillin
- Contraindications to oral surgery
- Treatment with immunosuppressive agents or immunocompromised status
- Treatment with amino-bisphosphonate and anti-angiogenetic medications
- Irradiation to head and neck area
- Uncontrolled diabetes
- Renal failure
- Drug and alcohol addiction
- Psychiatric disorders
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
U.O. Odontostomatologia e Chirurgia del Cavo Orale
Pisa, Italy, 56126
Actively Recruiting
Research Team
A
Antonio Barone, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
OTHER
Number of Arms
2
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