- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07665918
Evaluation of OMEGA-3 Effect in Alveolar Socket Preservation in Aesthetic Zone
June 18, 2026 updated by: Salma Khaled Elmetwally, Cairo University
Evaluation of OMEGA-3 Effect in Alveolar Socket Preservation in Aesthetic Zone: A Case Series
To evaluate the effect of Omega-3 in preserving bone after extraction
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The evaluation of the effect of omega-3 on the bone of the socket with changes in the dimensions like vertical and horizontal bone changes 3months after extraction .
Study Type
Interventional
Enrollment (Actual)
10
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Cairo, Egypt
- Faculty of Dentistry
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Description
Inclusion Criteria:
- Patients with non-restorable remaining roots.
- Patients free of systemic conditions that might affect the surgical procedure or the quantity or quality of bone (uncontrolled hypertension, uncontrolled diabetes).
Exclusion Criteria:
- Patients below 18 years old
- Patients with hypersensitivity to omega-3, drug formulations or allergic to seafood.
- Pregnant or lactating females
- Patients undergoing chemotherapy or radiotherapy
- Smokers
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Atraumatic extraction for single rooted teeth and placement of omega-3 in the socket
Atraumatic extraction for single rooted teeth in anterior zone and omega-3 polyunsaturated fatty acid placed with collagen sponge inside the extraction socket for socket preservation and implant placement
|
omega-3 fatty acid supplement
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Post-operative pain
Time Frame: immediately after extraction and the second day after extraction
|
Visual Analogue Scale score "VAS score" From 0-10 scores score 0 is no pain which is the best 1-4 is mild pain 5 is moderate pain from 5 -10 pain is getting worse and 10 is the worst
|
immediately after extraction and the second day after extraction
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Radiographic bone changes "horizontal bone changes " using Cone beam CBCT
Time Frame: before extraction and 3months after omega 3 placement
|
Performing one CBCT before extraction and one new CBCT after 3 months of extraction and omega-3 placement then comparing both CBCTs by J image computer program to get the difference in vertical bone measurements in millimeter
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before extraction and 3months after omega 3 placement
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Radiographic bone changes " Vertical bone fill" using CBCT
Time Frame: before and after 3 months of extraction and omega-3 placement
|
Performing one CBCT before extraction and one new CBCT after 3 months of extraction and omega-3 placement then comparing both CBCTs by J image computer program to get the difference in vertical bone measurements in millimeter
|
before and after 3 months of extraction and omega-3 placement
|
|
Radiographic bone changes "Bone density" using CBCT
Time Frame: 3 months after extraction and placement of omega-3
|
Performing one CBCT before extraction and one new CBCT after 3 months of extraction and omega-3 placement then comparing both CBCTs by J image computer program to get the radiographic bone changes in millimeter and Hounsfield units
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3 months after extraction and placement of omega-3
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Histological examination
Time Frame: after 3months of extraction during implant placement bone is taken using trephine bur
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using Hematoxylin and Eosin staining to measure the area of newly formed bone "Percentage"
|
after 3months of extraction during implant placement bone is taken using trephine bur
|
|
Healing Index "HI" by Landry et al using scores
Time Frame: after 3months of omega 3 placement
|
Using Landry et al wound healing index to measure soft tissue reaction changes.
Each category is scored from 1 to 5, with 1 indicating very poor healing and 5 indicating excellent healing.
The HI is a useful tool for assessing the quality of wound healing and guiding postoperative interventions.
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after 3months of omega 3 placement
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
January 1, 2025
Primary Completion (Actual)
October 24, 2025
Study Completion (Actual)
October 25, 2025
Study Registration Dates
First Submitted
May 27, 2026
First Submitted That Met QC Criteria
June 18, 2026
First Posted (Actual)
June 24, 2026
Study Record Updates
Last Update Posted (Actual)
June 24, 2026
Last Update Submitted That Met QC Criteria
June 18, 2026
Last Verified
June 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 30122024
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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