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Omega-3 Fatty AcidsNCT07665918

Evaluation of OMEGA-3 Effect in Alveolar Socket Preservation in Aesthetic Zone

A study testing Omega 3 Fish Oil supplements in people with Omega-3 Fatty Acids and Socket Preservation, run by Cairo University at 1 site in Egypt.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

To evaluate the effect of Omega-3 in preserving bone after extraction Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
What is being tested?
Omega 3 Fish Oil supplements
Could I receive a placebo?
No, everyone receives an active treatment
How many people
10 participants
Where
1 siteEgypt
Study dates
1 Jan 2025to 25 Oct 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Who may be able to join

  • 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).

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

Egypt1 site
  • Faculty of Dentistry

    Cairo

Other trials in Egypt

About this study

Official title: 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

Read the 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 .

Being tested
Omega 3 Fish Oil supplements
Keywords
Omega-3, Socket preservation, Atraumatic extraction, Esthetic zone, Extraction socket, Implant

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Omega 3 Fish Oil supplementsDietary supplement

    Also called Omega-3

    omega-3 fatty acid supplement

Study groups in NCT07665918
Study groupRoleWhat they receive
Atraumatic extraction for single rooted teeth and placement of omega-3 in the socketExperimentalAtraumatic 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
Receives: Dietary Supplement: Omega 3 Fish Oil supplements

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Post-operative pain

    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

    Measured: immediately after extraction and the second day after extraction

Secondary outcomes (5)
  1. Radiographic bone changes "horizontal bone changes " using Cone beam CBCT

    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

    Measured: before extraction and 3months after omega 3 placement

  2. Radiographic bone changes " Vertical bone fill" using CBCT

    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

    Measured: before and after 3 months of extraction and omega-3 placement

  3. Radiographic bone changes "Bone density" using CBCT

    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

    Measured: 3 months after extraction and placement of omega-3

  4. Histological examination

    using Hematoxylin and Eosin staining to measure the area of newly formed bone "Percentage"

    Measured: after 3months of extraction during implant placement bone is taken using trephine bur

  5. Healing Index "HI" by Landry et al using scores

    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.

    Measured: after 3months of omega 3 placement

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted24 Jun 2026
  2. Study start1 Jan 2025
  3. Primary completion24 Oct 2025
  4. Study completion25 Oct 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Prevention
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
10 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07665918
Sponsor's protocol ID
30122024
Status last verified
Jun 2026
First submitted
27 May 2026
Last updated
24 Jun 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Omega 3 Fish Oil supplements in people with Omega-3 Fatty Acids and Socket Preservation, run by Cairo University at 1 site in Egypt.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 Jun 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Egypt. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Post-operative pain (time frame: immediately after extraction and the second day after extraction). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Jun 2026.

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