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Clinical Trials in Egypt / NCT07700732
Active, not recruiting Not applicable

Photofunctionalization and Hyaluronic Acid for Posterior Maxillary Implants

NCT07700732 · tracked via the Priya Life Science Egypt tracker
Phase
Not applicable
Started
2025-10-01
Last updated
2026-07-14

Condition(s) studied

Tooth LossSurface TreatmentDelayed ImplantImplant PlacementUV Dental ImplantHyaluronic Acid (HA)

Investigational drug(s) / intervention(s)

Delayed dental implant placement without photofunctionalization.Delayed dental Implant photofunctionalization before placementDelayed dental Implant photofunctionalization and hyaluronic acid application before placement.

Delayed dental implant placement without photofunctionalization.: Delayed dental implants placed without photofunctionalization or hyaluronic acid in the posterior maxilla.

Delayed dental Implant photofunctionalization before placement: Delayed dental implants photofunctionalized with UV light before placement in the posterior maxilla.

Delayed dental Implant photofunctionalization and hyaluronic acid application before placement.: Delayed dental implants photofunctionalized with UV light and treated with hyaluronic acid before placement in the posterior maxilla.

Study summary

This randomized clinical trial evaluates the effect of UV photofunctionalization and hyaluronic acid on dental implants placed in the posterior maxilla. Clinical and radiographic outcomes will be assessed during follow-up

Eligibility

Sex
ALL
Min age
18 Years
Max age
60 Years
Healthy volunteers
No
Inclusion Criteria: * Patients with missed single tooth or multiple teeth in posterior maxilla. * Patients Free from any para-functional habits. * Patient with Adequate inter-arch relation and inter-occlusal space to accommodate the prosthetic restoration. * Patient with good oral hygiene. * Patients Willing to participate in the study's follow-up intervals. Exclusion Criteria: * Patients with any local or systemic disease that absolute contraindicate implant placement or surgery. * Pregnancy. * Patients with any pathological lesion or aggressive periodontal disease at the planned surgical site. * Patients on drugs that could affect bone healing process such as bisphosphonate. * Heavy Smokers for more than 10 cigarettes a day. * Uncooperative patients.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Faculty of Dentistry Mansoura University Al Mansurah Egypt

More Mansoura University trials in Egypt

Other trials for the same condition

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 NCT07700732 on ClinicalTrials.gov ↗ ← All trials in Egypt