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Clinical Trials in Egypt / NCT07700914
Active, not recruiting Not applicable

Effect of Different Loading Protocols on Photofunctionalized Implants in the Posterior Maxilla

NCT07700914 · tracked via the Priya Life Science Egypt tracker
Sponsor
Mansoura University
Phase
Not applicable
Started
2026-01-01
Last updated
2026-07-14

Condition(s) studied

Tooth LossSurface TreatmentImmediate Dental Implant LoadingImplant LoadingImplant PlacementUV Dental Implant

Investigational drug(s) / intervention(s)

Immediate loading of UV-photofunctionalized dental implantsEarly loading of UV-photofunctionalized dental implantsConventional loading of UV-photofunctionalized dental implants

Immediate loading of UV-photofunctionalized dental implants: Immediate loading of UV-photofunctionalized dental implants placed in the posterior maxilla.

Early loading of UV-photofunctionalized dental implants: Early loading of UV-photofunctionalized dental implants placed in the posterior maxilla.

Conventional loading of UV-photofunctionalized dental implants: Conventional loading of UV-photofunctionalized dental implants placed in the posterior maxilla

Study summary

This randomized clinical trial evaluates different loading protocols for UV-photofunctionalized dental implants in the posterior maxilla. Clinical and radiographic outcomes will be assessed during follow

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 absolutely 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. * Smokers. * Uncooperative patients.

Primary outcome measure(s)

  • Implant Stability — -Immediately after impant placement -immediately after loading -3 months after loading - 6 months after loading
    Implant stability will be evaluated using Osstell device based on resonance frequency analysis (ISQ values).
  • Hard Tissue (peri-implant bone) — - Immediately Postoperative (baseline) - 3 months after loading. - 6 months after loading.
    Marginal bone loss will be assessed using CBCT measured in mm.

Trial sites (1)

FacilityCityRegionStatus
Faculty of Dentistry Mansoura University Al Mansurah Egypt

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Other trials for the same condition

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Evaluation of Enamel Matrix Derivative in Immediate Dental Implants in the Mandibular Molar Region Recruiting
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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 NCT07700914 on ClinicalTrials.gov ↗ ← All trials in Egypt