Assessment of Rapid Osseointegration of Dental Implants with Different Coatings

NCT ID: NCT06650280

Last Updated: 2024-10-21

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

45 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-02-01

Study Completion Date

2024-06-01

Brief Summary

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The study will assess early osseointegration of dental implant with three different coating materials through secondary implant stability

Detailed Description

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Dental implants with sandblasted acid itched coating, nano-hydroxyapatite coating, and hyalouronic acid coating will be placed in the posterior maxilla to restore a missing tooth. Implant stability by the use of Ostell will be measured immediately post-operative, 4, 6, and 12 weeks post-operative.

marginal bone loss around the implants will be compared immediately after final restoration delivery and after one year

Conditions

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Dental Implants Hyaluronic Acid

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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sandblasted acid etched group

sandblasted acid etched coated implants will be allocated to this arm

Group Type EXPERIMENTAL

sandblasted acid etched

Intervention Type OTHER

SLA coated implants will be placed in posterior maxilla and implant stability will be evaluated

nano-hydroxyapatite group

nano-hydroxyapatite coated implants will be allocated to this arm

Group Type ACTIVE_COMPARATOR

nano-hydroxyapatite

Intervention Type OTHER

nano-hydroxyapatite coated implants will be placed in posterior maxilla to assess rapid osseointegration

hyaluronic acid group

hyaluronic acid coated implants will be allocated to this arm

Group Type EXPERIMENTAL

Hyaluronic Acid (HA)

Intervention Type OTHER

hyaluronic acid coated implants will be placed in posterior maxilla to evaluate rapid osseointegration

Interventions

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Hyaluronic Acid (HA)

hyaluronic acid coated implants will be placed in posterior maxilla to evaluate rapid osseointegration

Intervention Type OTHER

nano-hydroxyapatite

nano-hydroxyapatite coated implants will be placed in posterior maxilla to assess rapid osseointegration

Intervention Type OTHER

sandblasted acid etched

SLA coated implants will be placed in posterior maxilla and implant stability will be evaluated

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. Patients with missing at least one maxillary posterior tooth
2. Patients free from any systemic disease
3. Patients who approve to be included in the trial and sign the informed consent
4. Patients with no intra-bony defect.
5. Adults aged 18 years old and above

Exclusion Criteria

1. Patients who are allergic to titanium
2. Heavy smoker patient
3. Patients receiving chemotherapy or radiotherapy
4. Patients who refused to be included in the trial
Minimum Eligible Age

18 Years

Maximum Eligible Age

49 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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October University for Modern Sciences and Arts

OTHER

Sponsor Role lead

Responsible Party

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Mohamed Hamdy Mahmoud Ismail

Lecturer of Oral & Maxillofacial Surgery

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mohamed Hamdy, Lecturer

Role: PRINCIPAL_INVESTIGATOR

Faculty of Dentistry, MSA University, Egypt

Locations

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Faculty of Dentistry, MSA University

Giza, , Egypt

Site Status

Countries

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Egypt

References

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Atsumi M, Park SH, Wang HL. Methods used to assess implant stability: current status. Int J Oral Maxillofac Implants. 2007 Sep-Oct;22(5):743-54.

Reference Type BACKGROUND
PMID: 17974108 (View on PubMed)

Other Identifiers

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31910-4

Identifier Type: -

Identifier Source: org_study_id

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