Assessment of Osseointegration Properties of Nano-Hydroxy Apatite Coated Titanium Implant

NCT ID: NCT05936775

Last Updated: 2024-04-09

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

2023-06-22

Study Completion Date

2024-04-05

Brief Summary

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the purpose of this trial is to evaluate the osseointegration properties of nano-hydroxy apatite coated titanium implants in posterior maxilla. 30 patients will be included in this trial divided into two groups, control and intervention. Primary and secondary implant stability will be measured

Detailed Description

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Conditions

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Implant Site Reaction

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Nano-hydroxy apatite arm

in this groups patients will receive nano-hydroxy apatite coated titanium implants

Group Type EXPERIMENTAL

nano-hydroxy apatite coated titanium implants

Intervention Type OTHER

titanium implants with surface treatment of nano-hydroxy apatite

SLA arm

in this group patients will receive sandblasted large thread acid etched titanium implants

Group Type ACTIVE_COMPARATOR

sandblasted large acid itched coated titanium implant

Intervention Type OTHER

titanium implants with SLA surface treatment

Interventions

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nano-hydroxy apatite coated titanium implants

titanium implants with surface treatment of nano-hydroxy apatite

Intervention Type OTHER

sandblasted large acid itched coated titanium implant

titanium implants with SLA surface treatment

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

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Mohamed H Mahmoud, PhD

Role: PRINCIPAL_INVESTIGATOR

october university for modern science and arts faculty of dentistry

Locations

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October University for Modern Sciences and Arts faulty of Dentistry

Giza, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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2

Identifier Type: -

Identifier Source: org_study_id

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