NCT07549672

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

75
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
100

participants targeted

Target at P75+ for early_phase_1 pain

Timeline
4mo left

Started Jul 2023

Longer than P75 for early_phase_1 pain

Geographic Reach
1 country

1 active site

Status
active not recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress90%
Jul 2023Sep 2026

Study Start

First participant enrolled

July 1, 2023

Completed
2.8 years until next milestone

First Submitted

Initial submission to the registry

April 9, 2026

Completed
15 days until next milestone

First Posted

Study publicly available on registry

April 24, 2026

Completed
3 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Expected
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2026

Last Updated

April 28, 2026

Status Verified

April 1, 2026

Enrollment Period

3.1 years

First QC Date

April 9, 2026

Last Update Submit

April 23, 2026

Conditions

Keywords

Dry socketPainLower third molar

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

EXPERIMENTAL

study group

Drug: Ozone Oil-based Gel

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

Also known as: CHX Gel
study group and control group

Eligibility Criteria

Age21 Years - 35 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

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

Study Sites (1)

ASSOCIATE PROFESSOR cairo university

Cairo, Cairo Governorate, 12515, Egypt

Location

MeSH Terms

Conditions

PainDry Socket

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsMouth DiseasesStomatognathic Diseases

Study Design

Study Type
interventional
Phase
early phase 1
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Model Details: 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
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

Locations