Surgical Guided Fabricated From Two Different Printing Materials

NCT ID: NCT06628492

Last Updated: 2024-10-08

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

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

12 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-10-31

Study Completion Date

2024-11-30

Brief Summary

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implant will be inserted in patients with kennedy class 3 or 4 partially edentulous mandible .the implants will be inserted using teeth supported surgical guide fabricated from two different materials

Detailed Description

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Conditions

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Partial-edentulism

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Investigators Outcome Assessors

Study Groups

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group A implant inserted by stainless steel surgical guide

Group Type EXPERIMENTAL

stainless steel printed surgical guide

Intervention Type DEVICE

the patient will wear the stainless steel surgical guide for the insertion of one implant

group B implant inserted by resin surgical guide

Group Type ACTIVE_COMPARATOR

resin printed surgical guide

Intervention Type DEVICE

the patient will wear the resin surgical guide for insertion of adjacent another implant implant

Interventions

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stainless steel printed surgical guide

the patient will wear the stainless steel surgical guide for the insertion of one implant

Intervention Type DEVICE

resin printed surgical guide

the patient will wear the resin surgical guide for insertion of adjacent another implant implant

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

1. Patients with skeletal Angle“s class I maxilla-mandibular relationship,
2. adequate inter-arch distance, have Kennedy class 3 or 4 partially edentulous mandible of more than 2 teeth missed and will be applied for the treatment of tooth loss and requiring fixed prosthodontic rehabilitation
3. normal Physical and psychological status to tolerate conventional implant procedures,
4. Their residual ridge had sufficient bone volume for implant installation and was covered by firm mucoperiosteum.

Exclusion Criteria

1. Smokers.
2. Patients undergoing chemotherapy or radiotherapy and immunocompromised patients.
3. Patients with, systemic disease that might complicate post-operative healing or contribute to bone resorption, e.g uncontrolled diabetes, psychological disorders, or alcohol, tobacco, or drug abuse
4. parafunctional habits, poor oral hygiene, limited mouth opening, severe alveolar bone deficiencies,
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Suez Canal University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Central Contacts

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ahmed m hebeshi, Phd

Role: CONTACT

00201282531256

Other Identifiers

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802/2024

Identifier Type: -

Identifier Source: org_study_id

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