Effect of Hyaluronic Acid, With Demineralized Tooth Graft, in Socket Preservation, vs Demineralized Tooth Graft Alone.

NCT ID: NCT05613075

Last Updated: 2025-06-05

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-12-01

Study Completion Date

2024-11-29

Brief Summary

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Many dentists, clinicians and researchers have conducted numerous trials, and put several materials and procedures under the test, in an attempt to preserve vertical and/or horizontal extraction sockets dimensions. The clinical consequences of post-extraction remodeling may affect the outcome of the ensuing therapies aimed at restoring the lost dentition, either by limiting the bone availability for ideal implant placement or by compromising the aesthetic result of the prosthetic restorations. In an attempt for ridge/socket preservation of a freshly extracted tooth socket/bed, this study aims to assess and compare between using autogenous tooth graft added with Hyaluronic acid, and the usage of the standardized autogenous tooth graft alone, regarding the potency, preservative feature, and quality of bone healing, density, and deposition. For a better restorative outcome using a delayed implant placement later on in the edentulous area.

Detailed Description

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The available studies provide insufficient information to assess the efficacy of the usage of ha after tooth extraction in order to induce wound healing and accelerates bone deposition and differentiation. Hence, the purpose of this clinical trial is to investigate whether there is any beneficial value of local administration of 8% ha gel formulation (gengigel ®; farmalink saglik, istanbul, turkey) on the postoperative healing phase, bone density and ridge dimensions.

In an attempt for ridge/socket preservation of a freshly extracted tooth socket/bed, this study aims to assess and compare between using autogenous tooth graft added with Hyaluronic acid, and the usage of the standardized autogenous tooth graft alone, regarding the potency, preservative feature, and quality of bone healing, density, and deposition. For a better restorative outcome using a delayed implant placement later on in the e-dentulous area.

Our null hypothesis that post-extraction ridges preserved with Hyaluronic acid mixed with autogenous tooth grafts will present no significant higher bone density at extraction site, nor better dimensional preservation of the ridge tooth/teeth socket(s), vertically and/or horizontally, than the normalized/standardized ridge preservation using autogenous tooth graft particulates alone, carried to serve delayed implants placement later on, at extraction sites.

Conditions

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Alveolar Bone Resorption Socket Preservation Bone Resorption Unrestorable Dentition

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Outcome Assessors

Study Groups

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tooth extraction and socket preservation with demineralized tooth graft

patients with immediate extraction sockets, filled and condensed with demineralized, autogenous dentinal graft particles, extracted and originated from the newly extracted tooth, then covered with biodegradable Gel foaming sponge.

Group Type ACTIVE_COMPARATOR

tooth extraction and socket preservation with demineralized tooth graft

Intervention Type PROCEDURE

tooth extraction and socket preservation with demineralized tooth graft

tooth extraction and socket preservation with demineralized tooth graft and hyaluronic acid

patients with immediate extraction sockets, filled and condensed with demineralized, autogenous dentinal graft particles, extracted and originated from the newly extracted tooth, mixed with Hyaluronic acid, in gel form, as a carrier, then covered with biodegradable Gel foaming sponge.

Group Type EXPERIMENTAL

tooth extraction and socket preservation with demineralized tooth graft with hyaluronic acid

Intervention Type PROCEDURE

tooth extraction and socket preservation with demineralized tooth graft with hyaluronic acid

Interventions

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tooth extraction and socket preservation with demineralized tooth graft

tooth extraction and socket preservation with demineralized tooth graft

Intervention Type PROCEDURE

tooth extraction and socket preservation with demineralized tooth graft with hyaluronic acid

tooth extraction and socket preservation with demineralized tooth graft with hyaluronic acid

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* 1\. 18 years old or older.
* 2\. Requiring alveolar preservation after tooth extraction prior to placement of dental implant.
* 3\. Participants that are eligible for immediate implantation, yet having factors that are hindering these patients from immediate placement of an implant at the time of extraction (ex: Financial related factors - psychological factors - time related factors).
* 4\. Motivated patients with good enough understanding of oral health measurements and importance.
* 5\. Sufficient keratinized gingiva to cover the grafted bone. 6. The presence of dentition adjacent to the bone defect.
* 7\. Patients who are healthy or have well-controlled systemic disease(s).
* 8\. Teeth extractions are to be recommended due to trauma, caries, or periodontal diseases. \* 9. Single rooted teeth from both arches.
* 10\. No acute infections, pus formation, socket and bony discharges.
* 11\. Hopeless teeth, to be extracted, are bounded both mesially and distally by adjacent, teeth.
* 12\. Intact buccal bone of the teeth to be extracted.

Exclusion Criteria

* 1\. Heavy smokers (more than 10 cigarettes per day or an electronic cigarette dose of \>6 mg/ml of nicotine).
* 2\. Presence of active infection or severe inflammation in the intervention zone.
* 3\. Relevant medical history that contraindicates implant surgery.
* 4\. Immunosuppression (eg. Hiv, solid-organ transplants). 5. Head and neck-irradiated patients in the past 5 years. 6. Regular intake of bisphosphonates, anticoagulants, or anti-inflammatories.
* 7\. Chronic drug abuse or alcoholic habits. 8. Patients with poor oral hygiene (full-mouth plaque score and full-mouth bleeding score \>15%) and lack of motivation.
* 9\. Uncontrolled diabetes (reported levels of glycated haemoglobin exceeding 7%).
* 10\. Uncontrolled and /or untreated periodontal disease. 11. Patients who had previously received bone graft on the site to be operated. 12. Patients with significant comorbidity such as recent heart attack or coagulation disorder.
* 13\. Pregnant subjects.
Minimum Eligible Age

21 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Rahma Hesham Ahmed

dentistry post graduate master student, Implantology Department

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Rahma H Mohamed Ali

Role: PRINCIPAL_INVESTIGATOR

Cairo University, Faculty of Dentistry

Locations

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Cairo university

Cairo, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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rahma.autograft

Identifier Type: -

Identifier Source: org_study_id

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