Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07433322

Alveolar Ridge Preservation in the Posterior Maxilla: Clinical and Economic Evaluation After Extraction of Maxillary Molars

Led by Virginia Commonwealth University · Updated on 2026-04-27

40

Participants Needed

1

Research Sites

4 weeks

Total Duration

On this page

Sponsors

V

Virginia Commonwealth University

Lead Sponsor

D

Dentsply Sirona Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are evaluating alveolar ridge preservation (ARP) in the posterior maxilla after the extraction of maxillary molars to address bone and soft tissue loss that occurs following tooth removal. This study focuses on improving implant therapy by examining whether immediate or delayed grafting better supports bone and soft tissue maintenance, considering challenges like sinus pneumatization and dimensional changes in the extraction site. The research is conducted by Virginia Commonwealth University using a multidisciplinary model combining periodontics and prosthodontics expertise. The study compares two grafting approaches: immediate grafting using Ossix Plus membrane and Ossix bone graft right after tooth extraction, and delayed grafting performed at the time of implant placement using Ossix Agile membrane and Ossix bone graft if needed. Both materials are FDA approved and used according to manufacturers' instructions in standard care. Treatment plans are personalized based on preoperative analysis to reduce the number of grafting procedures while aiming for ideal implant positioning. Participants will be followed up at 2 weeks, 6 months, and 1 year after implant placement to assess patient-reported outcomes using the Oral Health Impact Profile-14 (OHIP-14) and clinical and radiographic measures such as bone thickness, soft tissue thickness, sinus pneumatization, bone height and width, and marginal bone levels. The study includes thorough surgical and prosthetic planning, digital workflows, and continuous patient monitoring to evaluate the clinical and economic effectiveness of ARP strategies in a controlled academic setting.

CONDITIONS

Brief Title

Alveolar Ridge Preservation (ARP) in the Posterior Maxilla After the Extraction of Maxillary Molars

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Intact or less than 5 mm dehiscence on the buccal and palatal sides
  • Initial residual bone height of at least 6 mm
  • Minimum distance of 1 mm between root apices and sinus membrane
  • Age 18 years or older
  • Medically healthy to undergo the procedure
Not Eligible

You will not qualify if you...

  • Medically compromised individuals
  • Heavy smokers
  • Individuals younger than 18 years
  • Those refusing treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - From extraction until implant placement, timing varies by participant

Participants undergo tooth extraction and receive either immediate bone grafting at the extraction site or delayed grafting at the time of implant placement according to their assigned group.

1 visit for extraction and grafting or 1 visit for extraction and later grafting at implant placement

Post-operative Follow-up

Duration - Up to 1 year after implant placement

Participants are followed after implant placement to monitor healing, bone and soft tissue outcomes, and patient-reported experiences.

Visits at 2 weeks, 6 months, and 1 year post-implant

Trial Site Locations

Total: 1 location

1

Virginia Commonwealth University

Richmond, Virginia, United States, 23298

Actively Recruiting

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Research Team

I

Iya Ghassib

T

Tara Zhou

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

OTHER

Number of Arms

2

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