Actively Recruiting
Efficacy of Ozone Therapy in Reducing Complications Following Impacted Mandibular Third-molar Surgery
Led by Jelena Krunic · Updated on 2025-01-31
20
Participants Needed
1
Research Sites
21 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this clinical trial is to learn if use of ozone works to treat complications after impacted mandibular third molar surgery. It will also learn does ozone has positive effect on wound healing and quality of life. The main questions it aims to answer are: * Does ozone reduce incidence of postoperative compliactions such as pain, swelling or reduced mouth opening after impacted mandibular third molar surgery? * Does ozone improve wound healing after impacted mandibular third molar surgery? * Does ozone have positive effect on quality of life after impacted mandibular third molar surgery? Participants will: * Receive ozone after impacted mandibular third molar surgery. * Visit the clinic 1st, 3rd, and 7th days after the intervention for checkups and tests. * Keep a diary of their symptoms.
CONDITIONS
Official Title
Efficacy of Ozone Therapy in Reducing Complications Following Impacted Mandibular Third-molar Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients over 18 years
- Patients with bilaterally impacted mandibular third molars classified as impaction index II B
- Patients in good general health (ASA classification I or II)
You will not qualify if you...
- Contraindications for ozone application including pregnancy, hyperthyroidism, favism, anemia, myasthenia, bleeding disorders, alcohol intoxication, myocardial infarction, pacemaker, or allergy to ozone
- Use of corticosteroid or antibiotic therapy in the last three months
- Signs of local inflammation in the oral cavity
- Female patients who are pregnant or breastfeeding
AI-Screening
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Trial Site Locations
Total: 1 location
1
University of East Sarajevo, Faculty of Medicine
Foca, Republika Srpska, Bosnia and Herzegovina, 73300
Actively Recruiting
Research Team
J
Jelena Krunic, Professor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
QUADRUPLE
Allocation
RANDOMIZED
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
2
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