Alveolar Ridge Augmentation Using Minimally Invasive Subperiosteal Tunneling With Xenogenic Bone Graft and PRF

NCT ID: NCT07079917

Last Updated: 2025-07-23

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

16 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-08-01

Study Completion Date

2026-06-21

Brief Summary

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surgical horizontal augmentation for maxillary alveolar ridge using minimally invasive subperiosteal tunneling in comparison to conventional surgical technique

Detailed Description

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Conditions

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Alveolar Bone Loss

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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subperiosteal tunneling for horizontal alveolar ridge augmentation

subperiosteal dissection through horizontal incision

Group Type ACTIVE_COMPARATOR

subperiosteal tunneling for horizontal alveolar ridge augmentation

Intervention Type PROCEDURE

subperiosteal dissection through horizontal incision only

conventional surgical approach for horizontal alveolar ridge augmentation

conventional full thickness trapezoidal flap for alveolar ridge augmentation

Group Type ACTIVE_COMPARATOR

conventional alveolar ridge augmentation

Intervention Type PROCEDURE

horizontal alveolar ridge augmentation through trapezoidal flap

Interventions

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subperiosteal tunneling for horizontal alveolar ridge augmentation

subperiosteal dissection through horizontal incision only

Intervention Type PROCEDURE

conventional alveolar ridge augmentation

horizontal alveolar ridge augmentation through trapezoidal flap

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Adults over 18 years old seeking an implant-supported restoration with deficient horizontal posterior maxillary alveolar ridge, at area of one or two missed teeth of less than 5 mm buccolingual width.
* Minimum vertical height of 8 mm.
* Gingival tissue of healthy adequate keratinization, more than 2mm.

Exclusion Criteria

* The presence of uncontrolled diabetes or any other systemic condition which may complicate the surgical procedure or interfere with bone healing
* Radiotherapy to the head and neck region
* Chemotherapy within the last 12 months
* Uncontrolled periodontitis
* Smoking
* Bisphosphonate therapy
* Pregnancy
* Presence of periapical infection or lesion
Minimum Eligible Age

18 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Fayoum University

OTHER

Sponsor Role lead

Responsible Party

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Abanoub Maged Sobhy Morkos

Demonstrator at oral & maxillofacial department

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Fayoum University

Al Fayyum, , Egypt

Site Status

Countries

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Egypt

Other Identifiers

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will be ready at end of study

Identifier Type: -

Identifier Source: org_study_id

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