Assessment of Bone Volume Changes in Immediate Implant Placement Using Allograft Versus Xenograft in Mandibular Molars

N/ANot Yet RecruitingNCT06962878

Cairo University20 enrolled

Overview

Twenty recruited patients indicated for immediate implant placement in mandibular molar sites are divided into two groups, with each group containing ten patients. One group assigned for placement of xenograft after molar extraction and immediate implant placement, while the other group received allograft as space-filling material.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

SINGLE

Enrollment

Conditions

Bone Volume Immediate Implant With Bone Graft

Interventions

XenograftPROCEDURE

The jumping gap and surrounding space will be augmented and packed with Xenograft

AllograftPROCEDURE

The jumping gap and surrounding space will be augmented and packed with Allograft

Eligibility

Sex: ALLMin age: 25 YearsMax age: 40 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Patients with non-restorable mandibular molars * Both sexes with age range from 25 years to 40 years * Good oral hygiene * Adequate alveolar bone dimensions for implant replacement * Adequate bone volume after extraction to achieve primary stability of the immediate implant * Co-operative patient Exclusion Criteria: * Patients with any systemic disease as uncontrolled diabetes or osteoporosis * Heavy smokers with smokers more than 10 cigarettes per day * Pregnancy * Patients with any signs of active infection or pus formation * Patients undergoing chemotherapy or radiotherapy, immunocompromised patients

Locations (1)

Faculty of Dentistry, Cairo University

Cairo, Egypt

Outcomes

Primary Outcomes

Horizontal bone thickness in millimeters

Two CBCT images will be taken, one immediately after surgery (baseline) and the other at 6 months post-surgically

Time frame: 6 months postoperative

Secondary Outcomes

Vertical bone height in millimeters

Two CBCT images will be taken, one 2 days after surgery (baseline) and the other at 6 months post-surgically

Time frame: 6 months postoperative

Pain intensity

The pain will be recorded by participants at 1, 3, and 7 days after surgery using the Visual Analogue Scale (VAS), which ranges from 0 to 10. The minimum score is 0, indicating no pain, and the maximum score is 10, representing the worst possible pain. Higher scores on the VAS indicate worse outcomes in terms of pain experienced.

Time frame: One week postoperative

Central Contacts

Ahmed Mohamed Tawfik, BSc

CONTACT

+201095544285 ahmed-tawfik@dentistry.cu.edu.eg

Data from ClinicalTrials.gov

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