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Clinical Trial

Tissue Preservation in Immediate 1C Implants Using an Anatomical Prefabricated Healing Abutment

NCT: NCT07727980 · NOT_YET_RECRUITING

NCT IDNCT07727980
StatusNOT_YET_RECRUITING
Start Date2026-09
Completion2028-09
SponsorUniversity of Illinois at Chicago (OTHER)
First posted
Last updated

Brief Summary

The goal of this clinical trial is to evaluate whether an anatomical prefabricated healing abutment (AHA) improves tissue preservation and clinical outcomes following immediate implant placement after tooth extraction in adults. Although immediate implant placement is a well-established treatment for replacing missing teeth, healing can result in changes to the surrounding bone and soft tissues that may affect the esthetic appearance, function, and long-term stability of the implant-supported restoration. This study will compare an anatomical healing abutment, designed to mimic the natural tooth emergence profile and support peri-implant tissues during healing, with a conventional healing abutment. The primary objectives are to determine whether the AHA better preserves soft tissue contours and alveolar bone, improves implant positioning accuracy and tissue stability during healing, and differs from a conventional healing abutment in complications or adverse events. Eligible participants will be adults requiring extraction of a hopeless tooth in the posterior maxilla or mandible who are suitable candidates for immediate implant placement. Following tooth extraction and implant placement, participants will receive either an anatomical prefabricated healing abutment or a conventional healing abutment and will return for scheduled follow-up visits over approximately 12 months to assess healing, implant stability, and changes in the surrounding hard and soft tissues. Researchers will collect clinical measurements, digital intraoral scans, photographs, and radiographic images throughout the study. Additional research imaging will be used to generate three-dimensional models to measure tissue volume changes and implant position accuracy. Specialized software will compare changes between the two groups over time. Safety will be evaluated by monitoring participants for complications, discomfort, inflammation, implant-related problems, and other adverse events throughout follow-up. All procedures will be performed by trained dental professionals using established clinical protocols. The results may improve understanding of how healing abutment design influences tissue preservation after immediate implant placement and help optimize future implant therapy by supporting better functional, esthetic, and long-term outcomes.

Frequently Asked Questions

What is Tissue Preservation in Immediate 1C Implants Using an Anatomical Prefabricated Healing Abutment?

Tissue Preservation in Immediate 1C Implants Using an Anatomical Prefabricated Healing Abutment is a clinical trial registered under NCT07727980. Current status: NOT_YET_RECRUITING.

What is the status of NCT07727980?

The current status of NCT07727980 (Tissue Preservation in Immediate 1C Implants Using an Anatomical Prefabricated Healing Abutment) is: NOT_YET_RECRUITING.

When did Tissue Preservation in Immediate 1C Implants Using an Anatomical Prefabricated Healing Abutment start?

Tissue Preservation in Immediate 1C Implants Using an Anatomical Prefabricated Healing Abutment started on 2026-09.

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Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.