Interchangeable Guide in Ridge Splitting Flapless Technique for Implant Placement

NCT ID: NCT04386382

Last Updated: 2020-05-13

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

8 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-10-01

Study Completion Date

2020-05-01

Brief Summary

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A clinical trial was conducted to evaluate the accuracy of dental implant placement in narrow ridges after ridge splitting flapless technique using an interchangeable guide.

Detailed Description

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A sample was selected conveniently to fulfill a list of inclusion and exclusion criteria. Then the selected participants underwent ridge splitting with the aid of interchangeable guide. After ridge splitting, all patients had simultaneous implant placement followed by clinical and radiographical evaluation over a period of 6 months.

Conditions

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Anterior Maxillary Narrow Ridge

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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ridge splitting flapless technique using interchangeable guide

Fabrication of interchangeable surgical guide stent:

* Optical scanning of the dental casts was done using Ceramill map 400
* The treatment plan and the surgical stent were designed using Mimics Innovation Suite 19 ™ software
* Series of creating and designing special 3D virtual guide slits and boxes that can accommodate and precisely fit the tools used for the ridge splitting technique.

Group Type EXPERIMENTAL

ridge splitting flapless technique using interchangeable guide followed by implant placement

Intervention Type PROCEDURE

An informed consent is taken from all the patients

I. Presurgical phase:

1. Proper dental and medical history.
2. Scaling and oral hygiene measurements.
3. Clinical examination.
4. Radiographic examination. Clinical bucco-lingual measurements was done using calipers to ensure the patients would meet our initial inclusion criteria prior to further investigations.

III. Fabrication of interchangeable surgical guide stent from primary impression:

1. Optical scanning of the dental casts was done using Ceramill map 400
2. surgical stent was designed using Mimics Innovation Suite 19 ™ software.
3. Series of creating and designing special 3D virtual guide slits and boxes that can accommodate and precisely fit the tools used for the ridge splitting technique.

All patients will be operated under local anesthesia, stent was placed on ridge and adapted well after disinfection osteotomy was done using piezotome splitting tips Implant-insertion was started immediately

Interventions

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ridge splitting flapless technique using interchangeable guide followed by implant placement

An informed consent is taken from all the patients

I. Presurgical phase:

1. Proper dental and medical history.
2. Scaling and oral hygiene measurements.
3. Clinical examination.
4. Radiographic examination. Clinical bucco-lingual measurements was done using calipers to ensure the patients would meet our initial inclusion criteria prior to further investigations.

III. Fabrication of interchangeable surgical guide stent from primary impression:

1. Optical scanning of the dental casts was done using Ceramill map 400
2. surgical stent was designed using Mimics Innovation Suite 19 ™ software.
3. Series of creating and designing special 3D virtual guide slits and boxes that can accommodate and precisely fit the tools used for the ridge splitting technique.

All patients will be operated under local anesthesia, stent was placed on ridge and adapted well after disinfection osteotomy was done using piezotome splitting tips Implant-insertion was started immediately

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients with anterior maxillary narrow ridge
* Patients with adequate alveolar ridge bone height
* Age ranging from 20-40 years.
* Patients should have adequate oral hygiene
* Patients should be free of soft tissue or oral dental pathology
* Patients who accept to participate in the study.

Exclusion Criteria

* Patients suffering from relevant systemic and/or metabolic diseases
* Patients suffering from immunosuppressive and/or autoimmune diseases
* Heavy smokers.
Minimum Eligible Age

20 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Hams Hamed Abdelrahman

OTHER

Sponsor Role lead

Responsible Party

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Hams Hamed Abdelrahman

Assistant lecturer

Responsibility Role SPONSOR_INVESTIGATOR

Locations

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Outpatient Clinic of Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Alexandria University, Egypt

Alexandria, Azarita, Egypt

Site Status

Countries

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Egypt

Other Identifiers

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Ridge splitting

Identifier Type: -

Identifier Source: org_study_id

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