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ACTIVE NOT RECRUITING
NCT07868744
NA

Clinical Assessment of UV Photofunctionalization on Stability and Osseointegration of Early Loaded Implants

Sponsor: Future University in Egypt

View on ClinicalTrials.gov

Summary

The goal of this clinical trial is to learn if UV light treatment (photo functionalization) works to help dental implants heal faster and become stable enough for early use in adults missing teeth in the lower back jaw. It will also learn about the survival rate and safety of these implants. The main questions it aims to answer are: Do the UV-treated implants achieve the required stability score (IST ≥ 65) at 4 to 6 weeks to allow for early placement of the artificial tooth? What are the implant survival rates, and how do the gums and surrounding bone respond 6 months after the artificial tooth is placed? Researchers will test the stability of these UV-treated implants against a standard clinical threshold to see if they safely support an early treatment timeline. Participants will :Have a UV-treated titanium dental implant surgically placed in their lower jaw. Visit the clinic for check ups and non-invasive stability tests at 2 weeks, 4 weeks, and 6 weeks after surgery. Receive their final artificial tooth between 4 to 6 weeks, provided the implant is completely stable. Return for follow-up X-rays and tissue checks at 1, 3, and 6 months after receiving the artificial tooth.

Official title: Clinical Assessment of UV Photofunctionalization on Stability and Osseointegration of Early Loaded Implants A Prospective Clinical Study

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

18

Start Date

2026-04-01

Completion Date

2027-03-30

Last Updated

2026-10-09

Healthy Volunteers

Yes

Interventions

DEVICE

UV-photofunctionalized titanium dental implants

Unlike standard titanium implants that are placed directly from the packaging, the implants in this study (Point UV® Implant System, Titanium Grade 4) undergo Ultraviolet Photofunctionalization (UV phF) immediately prior to surgical insertion to activate the implant surface. The surgical placement is strictly limited to healed edentulous ridges located specifically in the mandibular posterior area (lower jaw).The intervention is exclusively performed on patients categorized as having D2 or D3 bone quality, verified by pre-operative CBCT scans. The intervention employs an early loading prosthetic protocol, distinguishing it from conventional/delayed loading approaches.

Locations (1)

Future university hospital

Cairo, Fifth Settlement, Egypt