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Clinical Trials/NCT02330822
NCT02330822
Completed
Not Applicable

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

Damascus University1 site in 1 country20 target enrollmentDecember 2014

Overview

Phase
Not Applicable
Intervention
Hyaluronic Acid
Conditions
Patients With Dental Extraction
Sponsor
Damascus University
Enrollment
20
Locations
1
Primary Endpoint
Vertical bone fill
Status
Completed
Last Updated
10 years ago

Overview

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

Registry
clinicaltrials.gov
Start Date
December 2014
End Date
September 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

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

Arms & Interventions

Hyaluronic Acid Group

In this Group, Hyaluronic acid will be injected following extraction.

Intervention: Hyaluronic Acid

Outcomes

Primary Outcomes

Vertical bone fill

Time Frame: This 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.

Change in bone mineral density (BMD)

Time Frame: (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.

Secondary Outcomes

  • Buccolingual distance(at six months post-extraction)
  • Mesiodistal distance(at six months post-extraction)

Study Sites (1)

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