Ozone Oil-based Gel and CHX Gel After Lower Third Molar Removal
Comparing Ozone Oil-based Gel and CHX Gel Applications to Reduce Pain and Incidence of Dry Socket After Lower Third Molar Extraction, a Randomized Clinical Study
1 other identifier
interventional
100
1 country
1
Brief Summary
Overall, 100 patients of both genders were included in the study, with indication of surgical extraction of lower third molar, positioned similarly after being clinically and radiographically checked by X-ray and orthopantomography. Each patient was subjected to both groups in separate sessions: treated with ozone gas and with CHX gel 1%. Data on pain intensity, number of taken analgesics- painkillers, and dry socket were recorded for 48 h and at Day 7
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for early_phase_1 pain
Started Jul 2023
Longer than P75 for early_phase_1 pain
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2023
CompletedFirst Submitted
Initial submission to the registry
April 9, 2026
CompletedFirst Posted
Study publicly available on registry
April 24, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2026
April 28, 2026
April 1, 2026
3.1 years
April 9, 2026
April 23, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
pain severity
pain scale ( VAS ; visual analogue scale) (1-10)
7 days
Secondary Outcomes (1)
dry socket incidence
15 daays
Study Arms (1)
study group and control group
EXPERIMENTALstudy group
Interventions
Overall, 30 patients of both genders were included in the study, with indication of surgical extraction of lower third molar, positioned similarly after being clinically and radiographically checked by X-ray and orthopantomography. Each patient was subjected to both groups in separate sessions: treated with ozone gas and with CHX gel 1%. Data on pain intensity, number of taken analgesics- painkillers, and dry socket were recorded for 48 h and at Day 7
Eligibility Criteria
You may qualify if:
- Patients with third impacted bilateral molars, symmetrically in the same position, position evaluated by radiography.
- Patients in whom operative extraction of third molars is indicated with the creation of a mucoperiosteal flap.
- Patients regardless of gender.
You may not qualify if:
- lack of cooperation in any of the work phase
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
ASSOCIATE PROFESSOR cairo university
Cairo, Cairo Governorate, 12515, Egypt
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- early phase 1
- Allocation
- NA
- Masking
- NONE
- Purpose
- PREVENTION
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- associate professor of oral and maxillofacial surgery
Study Record Dates
First Submitted
April 9, 2026
First Posted
April 24, 2026
Study Start
July 1, 2023
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
September 1, 2026
Last Updated
April 28, 2026
Record last verified: 2026-04
Data Sharing
- IPD Sharing
- Will not share