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Role of Hyaluronic Acid in Bone Healing After Dental Extraction

A Clinical and Experimental Study to Evaluate the Efficacy of Locally Applied Hyaluronic Acid in Bone Healing Following Dental Extraction

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02330822
Enrollment
20
Registered
2015-01-05
Start date
2014-12-31
Completion date
2015-09-30
Last updated
2015-09-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patients With Dental Extraction

Brief summary

This is a randomized controlled trial with a split mouth design. Patients with an indication of lower dental extraction will be asked to join this research project at the Department of Oral and Maxillofacial Surgery at University of Damascus Dental School. Each patient whose case requires bilateral extraction, one side will serve as an experimental side, whereas the other side will serve as a control. Participants should have symmetric teeth that need extraction in the lower jaw. Hyaluronic acid will be injected following extraction in one of the two sides with random allocation. cone-beam computerized tomography (CBCT) images will be taken for each participant immediately post-extraction and at six months post-operatively.

Detailed description

I- Clinical examination variables: Buccolingual distance and distomesial distance will be measured for each participant at 2 assessment times: directly post-extraction and six months post-extraction. II- Radiographic examination variables: Linear measurements Vertical bone fill Bone mineral density

Interventions

DRUGHyaluronic Acid

This material is going to be injected into the extraction socket in order to promote bone healing.

Sponsors

Damascus University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-60 years old * Symmetric teeth requiring extraction in the lower jaw * Systematically healthy

Exclusion criteria

* Smokers * Pregnancy (for female participants) * Diabetic patients * Patients with metabolic problems

Design outcomes

Primary

MeasureTime frameDescription
Change in bone mineral density (BMD)(BMD) will be measured two times in this study: directly at the day of extraction and six months post-extraction.BMD is the amount of bone tissue in a certain volume of bone. This variable is going to be measured on CBCT images.
Vertical bone fillThis variable is going to be measured at 6 months post-extraction'Vertical bone fill' is the distance between the base of the extraction socket and cement-enamel junction directly after extraction and minus the distance between base of the extraction socket and cement-enamel junction six months post-extraction. This variable is going to be measured on CBCT images.

Secondary

MeasureTime frameDescription
Buccolingual distanceat six months post-extractionBuccolingual distance is the distance between buccal wall and lingual wall of the extraction socket. This variable is going to be measured clinically.
Mesiodistal distanceat six months post-extractionMesiodistal distance is the distance between mesial wall and distal wall of the extraction socket. This variable is going to be measured clinically.

Countries

Syria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026