Skip to content

Immediate Implant in Posterior Mandible Region

Immediate Implant Placement Using Xenograft as Space Filling Material Mixed With Platelet-Rich Fibrin (PRF) Versus Hyaluronic Acid in Posterior Mandible Region

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07027904
Enrollment
24
Registered
2025-06-19
Start date
2025-06-12
Completion date
2026-08-01
Last updated
2025-06-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Immediate Implant With Bone Graft

Brief summary

This study aims to evaluate implant stability and Width bone after placement of immediate implant and Xenograft mixed with Hyaluronic acid or with Platelet-Rich Fibrin (PRF) at posterior mandible region

Interventions

DEVICEImplant

The immediate implant was placed, and the surrounding cavity was filled with xenograft bone material, along with the application of hyaluronic acid or platelet-rich fibrin (PRF) to enhance healing and bone integration.

Sponsors

WASIM MHD JEHAD HALABI
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* • Age ≥ 18 years. * Both sexes. * Cooperative and likely to maintain good dental health. * Recent extraction multi roots. * There is a bone between (2 or 3) mm at lest from the apex of the root.

Exclusion criteria

* • Patients who had undergone previous extraction of all badly decayed teeth . * Implant placement in both healed bone and at the extraction sites in the same procedure. * Presence of any local or systemic factors that might contraindicate oral surgery. * Poor oral hygiene. * Conditions that complicate wound healing such as uncontrolled diabetes, smoking (10 cigarettes a day), pregnancy, a history of drug or alcohol abuse, and an inability or unwillingness to return for follow-ups after occlusal loading.

Design outcomes

Primary

MeasureTime frameDescription
Implant secondary stability6 monthsMethod of Measurement (Using the Osstell® Device.) -Unit of Measurement (ISQ)

Secondary

MeasureTime frameDescription
width boneimmediate postoperative and at 6 monthsMethod of Measurement (Conebeam computed tomography (CBCT) ) -Unit of Measurement (Hounsfield unit)

Contacts

Primary ContactWASIM HALABI, MSc degree candidate
wasim.halabi@dentistry.cu.edu.eg+201152922450

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026