🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Egypt / NCT06207617
Recruiting Not applicable

Dimensional Changes Following Immediate Implant Placement in Molar Extraction Sockets With or Without Bone Graft

NCT06207617 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2026-02-01
Last updated
2026-05-28

Condition(s) studied

Immediate Implants

Investigational drug(s) / intervention(s)

Immediate implant placement + customized healing abutmentImmediate implant placement + xenogeneic bone graft material + customized healing abutment

Immediate implant placement + customized healing abutment: Immediate implant placement in fresh extraction molar sites + customized healing abutment fabricated by adding flowable composite to the temporary cylindrical abutment mimicking the shape of the socket at the marginal gingiva, then it will be screwed to the implant. no grafting material included in this arm

Immediate implant placement + xenogeneic bone graft material + customized healing abutment: Immediate implant placement in fresh extraction molar sites + xenogenic bone graft + customized healing abutment fabricated by adding flowable composite to the temporary cylindrical abutment mimicking the shape of the socket at the marginal gingiva, then it will be screwed to the implant.

Study summary

Statement of problem: The majority of studies on immediate implant placement are related to the maxillary esthetic zone. Literature concerning Immediate implant placement in the posterior region is scarce. Furthermore, there is paucity of evidence on alveolar bone dimensional changes following immediate implant placement in fresh extraction sockets of posterior teeth. Adding to that, negligible evidence is known about the soft tissue alterations which take place during modeling and remodeling phases of socket healing process; regarding the molar sites. Nevertheless, Immediate installation into a molar socket raises an extra challenge for the clinicians, because of the different anatomical features of the extraction sockets compared to that of the single-rooted teeth in the anterior zone. In addition to, implant positioning difficulties; due to the amount of the residual inter-radicular bone after extraction. Aim of the study: To assess the bucco-lingual ridge collapse after immediate implant placement in lower 1st molar sites either with customized healing abutment only; or with xenogeneic bone graft and customized healing abutment. Materials and methods: The current study will include 28 non-restorable lower 1st molar teeth indicated for extraction in the posterior area. Patients will randomly be assigned into two equal groups: the test group; Immediate implant placement + customized healing abutment group and the control group; Immediate implant placement +bone graft+ customized healing abutment group. The presented trial will investigate the following outcomes: bucco-lingual ridge collapse as the primary outcome, together with mid-facial recession, total volume gain/loss, buccal soft tissue contour, bucco-lingual bone width, and vertical bone changes as the secondary outcomes after 12 months

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: * Adults from the age of 18 - 50 years of both genders. * Patients with non-restorable single bounded mandibular 1st molar tooth indicated for extraction. * Periodontally healthy patients with good oral hygiene. * Intact interradicular bone with 2-3 mm width, assessed by CBCT. * Thin buccal plate of bone (1 mm or less) among both of the mesial and distal root, assessed by CBCT. * Intact gingival tissue with at least 2 mm keratinized tissue. * Patients accepts to provide written informed consent. Exclusion Criteria: * Molar sites indicated for extraction with roots of close proximity to vital structures as inferior alveolar nerve. * Pregnant females. * Smokers as smoking is a contraindication for any plastic periodontal surgery (Khuller, 2009). * Handicapped and mentally retarded patients. * Patients undergoing chemotherapy and/or radiotherapy. * Presence of systemic disease that would affect wound healing. * Presence of active infection with soft tissue communication.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
International Dental Continuing Education Cairo Egypt Recruiting

More Misr International University trials in Egypt

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06207617 on ClinicalTrials.gov ↗ ← All trials in Egypt