Using Buccal Pad of Fat Free Tissue Transfer With Immediate Implant Placement

Alexandria University

Status

Unknown

Conditions

Dental Implant

Treatments

Procedure: Xenograft bone substitute (Osteo-biol)

Study type

Interventional

Funder types

Other

Identifiers

NCT04415619

Buccal pad of fat free tissue

Details and patient eligibility

About

Implants placed immediately after tooth extraction usually present challenges in obtaining soft tissue coverage with high risk of bacterial invasion, wound dehiscence and subsequently adverse effect on the success rate of the implant due to lack of primary soft tissue closure over the implant.

Different surgical methods have been described to achieve primary soft tissue closure in maxillary fresh socket, each having its advantages and disadvantages, based on that, buccal pad of fat can solve this soft tissue coverage problem with minimal complications and high success rate of the placed implants.The objective of this study is to evaluate the use of buccal pad of fat tissue with immediate implant placement in the posterior maxillary area.

Full description

Ten patients will be selected randomly from the outpatient clinic, Alexandria University seeking for an immediate implant placement. The sample will be selected to match the inclusion and exclusion criteria. It will be operated upon in the Oral and Maxillofacial Department, Faculty of Dentistry, Alexandria University. One stage surgery will include tooth extraction, placement of an immediate implant, bone grafting material and autologous soft tissue graft from the buccal pad of fat. Patients will be assessed clinically and radiographically to evaluate bone and soft tissue measurements.

Enrollment

10 estimated patients

Sex

All

Ages

20 to 45 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients age between 20-45 years with no gender predilection.
Patients with non-restorable maxillary posterior tooth which need to be extracted (premolar -molar region).
Patients with good oral hygiene.
Bony defects more than 2 mm during implant placement treated by bone substitute.
Patients fully capable to comply with the study protocol.

Exclusion criteria

Patients with any systemic disease affecting bone quality as uncontrolled diabetes.
Heavy smokers (more than 20 cigarettes per day).
Sites with acute oral infection.
Pregnant and lactating patients.
Untreated periodontal disease.
Previous chemotherapy or irradiation of the head and neck.
Inadequate interocclusal space.