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Assessment of a New Enhanced Xenograft in Open Maxillary Sinus Augmentation

NCT07737704 · Status: RECRUITING · Phase: PHASE2/PHASE3 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-07-30

No results posted yet for this study

Summary

Implant supported dental restorations are sometimes challenging with decreased bone height in the posterior maxilla. The goal of this study is to test an augmentation bone substitute in elevating the maxillary sinus floor; in terms of soft tissue reaction, formed bone height as well as structure.

Bone substitute will be compared to a graftless method of bone augmentation depending on participants' bodies forming bone in the defective area.

Participants will:

* Undergo lateral maxillary sinus floor elevation with bone substitute or graftless method.
* Record postoperative swelling and pain through the follow up period.
* Take radiographs for evaluation of the formed bone before placing dental implants.

Conditions

  • Maxillary Sinus Floor Augmentation
  • Maxillary Sinus Elevation
  • Bone Augmentation

Interventions

BIOLOGICAL

Xenograft

hydrogel-enhanced xenograft

OTHER

maxillary sinus membrane elevation and stabilization.

graftless augmentation of the maxillary sinus floor through membrane elevation and stabilization; tenting.

Sponsors & Collaborators

  • Misr International University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-08-10
Primary Completion
2027-06-10
Completion
2027-12-12

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07737704 on ClinicalTrials.gov