Clinical Evaluation of Stability of Implants Placed in Partially Edentulous Maxilla With Poor Bone Quality Via New Reverse Drilling Technique Versus Osteotome Technique.

NCT ID: NCT04541641

Last Updated: 2020-09-09

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

UNKNOWN

Clinical Phase

NA

Total Enrollment

28 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-10-01

Study Completion Date

2023-08-01

Brief Summary

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The study will compare between osteotome technique and New Reverse Drilling Technique in the placement of dental implant in posterior maxilla , primary outcome will be Implant stability that will be measured by Periotest device . follow up for 6 month.

secondary outcomes will be crestal bone loss , pain and swelling.

Detailed Description

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Conditions

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Dental Implant

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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osteotome group

Group Type EXPERIMENTAL

osteotome technique

Intervention Type PROCEDURE

a technique for dental implant placement by using the osteotome to condense the bone and create an osteotome rather than cutting the bone

New Reverse Drilling technique

Group Type EXPERIMENTAL

New Reverse Drilling technique

Intervention Type PROCEDURE

a new technique of dental implant drilling that promote osseodensification by rotating the drills anti-clockwise rather than clockwise to promote bone condensation rather than bone cutting

Interventions

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New Reverse Drilling technique

a new technique of dental implant drilling that promote osseodensification by rotating the drills anti-clockwise rather than clockwise to promote bone condensation rather than bone cutting

Intervention Type PROCEDURE

osteotome technique

a technique for dental implant placement by using the osteotome to condense the bone and create an osteotome rather than cutting the bone

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

1. Partially edentulous patients in the maxillary posterior region.
2. Systemically healthy patient.
3. Presence of proper inter-arch space for placement of the implant prosthetic part.
4. Sufficient bone height and width for implant placement (bone height ≥10mm and bone width ≥6mm).
5. Non-smoker.
6. Patients who are ≥ 20 years old.
7. Good oral hygiene.
8. Acceptance of a one year follow-up period.
9. Informed consent is provided by the patient.

Exclusion Criteria

1. Patients with systemic conditions that may interfere with implant stability,
2. Patients with local pathological defects related to the area of interest.
3. Unmotivated, uncooperative patients with poor oral hygiene.
4. Patients with habits that may jeopardize the implant longevity and affect the results of the study such as alcoholism or parafunctional habits.
5. Inadequate inter-arch space for implant prosthetic part
Minimum Eligible Age

21 Years

Maximum Eligible Age

50 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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Mostafa Magdy Awad

doctorate candidate

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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PER6-3-1

Identifier Type: -

Identifier Source: org_study_id

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