MedPath

Xenograft with or Without Erythropoietin in Immediate Dental Implant

Not Applicable
Not yet recruiting
Conditions
Hopeless Teeth
Interventions
Combination Product: Erythropoietin (EPO) with xenograft
Other: Xenograft alone
Registration Number
NCT06601400
Lead Sponsor
Cairo University
Brief Summary

The aim of this study is to evaluate changes in buccal bone thickness after immediate implant placement with xenograft mixed with erythropoietin in the anterior maxilla with a thin buccal bone

Detailed Description

PICO:

Population: Patients with non-restorable tooth in anterior maxilla with thin buccal bone (less than 1mm) Intervention: Immediate implant placement with Xenograft mixed with Erythropoietin.

Control: Immediate implant placement with Xenograft alone.

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
24
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Group A (Test)Erythropoietin (EPO) with xenograftImmediate implant placement with Xenograft mixed with Erythropoietin
Group B (Control)Xenograft aloneImmediate implant placement with Xenograft alone
Primary Outcome Measures
NameTimeMethod
Buccal bone thickness.1 year follow up period

by Cone Beam Computed Tomography (CBCT) in mm

Secondary Outcome Measures
NameTimeMethod
Crestal bone loss1 year follow up period

will be measured by Cone Beam Computed Tomography (CBCT) in mm

Soft tissue thickness.1 year follow up period

will be measured by Endodontic spreader with rubber stopper in mm

The pink esthetic score (PES)1 year follow up period

by taking photographs

Success and survival criteria1 year follow up period

the absence of mobility, the absence of acute or chronic peri-implant infection, the absence of radiolucency around the implant, without pocket probing depth (PPD) ≧ 5 mm, and without vertical bone loss ≧ 1.5 mm in the first year. The cases will be defined as failure if it can\'t reach any one of the success criteria

Bleeding on probing (BOP)1 year follow up period

According to presence (yes) or absence (No) of bleeding on probing

Pain score1, 3, and 7 days

by using Visual analogue scale from (0-10)

Full-mouth plaque score1 year follow up period

According to presence (yes) or absence(No) of plaque

Trial Locations

Locations (1)

Faculty of dentistry, Cairo university

🇪🇬

Giza, Egypt

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