Clinical trial Recruiting at 1 site Interventional Ages 18 to 60

Tenting the Schneiderian membrane of the maxillary sinus using titanium mesh

Official title: Clinical, Radiographic and Histologic Evaluation of Tenting the Schneiderian Membrane Using Titanium Mesh for Maxillary Sinus Lift Procedure: A Randomized Controlled Study

Run by Suez Canal University · NCT07035236 · Data updated 2026-11-12

This trial will test whether using titanium mesh to lift and tent the sinus membrane improves outcomes for patients needing maxillary sinus floor augmentation for dental implants.

Quick facts

Study typeInterventional
Ages18 Years to 60 Years
SexAll
Enrollment20 (estimated)
SponsorSuez Canal University
Academic / other
Drugs / interventionschemotherapy
Locations1 site (Ismailia)
StatusRecruiting
StartedJuly 15, 2025
Main results expectedOctober 2026
Study endsDecember 2026
Registry record updatedApril 24, 2026
Trial IDNCT07035236 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–60 with one or more posterior maxillary sites needing implant-supported restorations, alveolar bone height under 5 mm, good oral hygiene, and willing to consent are ideal candidates.

Probably not a fit

Patients who are medically compromised (for example uncontrolled diabetes or recent chemotherapy/radiation), have active sinus infection, heavy smokers, or untreated periodontal disease are unlikely to benefit or be eligible.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Twenty posterior maxillary edentulous sites requiring open sinus augmentation for staged dental implant placement will be treated and compared between two mechanical stabilization methods. One group will have the Schneiderian membrane elevated and tented with titanium mesh fixed by bone screws, while the control group will receive conventional stainless steel screws or pins placed bucco-palatally. Platelet-rich fibrin (PRF) will be placed at the elevated membrane site in both groups, and patients will be followed for healing and readiness for implant placement. The study focuses on surgical technique and local tissue response rather than systemic therapies.

Why it matters

Potential benefit: If successful, this approach could provide more reliable membrane support and better bone fill, making staged implant placement more predictable for patients with severe posterior maxillary atrophy.

How similar studies have gone: Membrane tenting and the use of various meshes have been reported in the surgical literature with mixed but sometimes promising results, while large-scale evidence specifically for titanium mesh in this application remains limited.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Adult male/female patients with age interval 18:60 years old.
* Patients with one or more teeth requiring implant supported dental restoration in atrophic maxilla.
* Alveolar bone height less than 5 mm at the defective site.
* Good oral hygiene.
* Patient's consensual agreement to be enrolled in the study.

Exclusion Criteria:

* Medically compromised patients with conditions contraindicating surgery (eg. uncontrolled diabetics, bisphosphonate intake, radio or chemotherapy).
* Patients with active infection at or related to the site of surgery (eg. acute sinusitis).
* Heavy smokers.
* Patients not indicated for an implant supported restoration at the time of enrollement (eg. active/untreated periodontal disease). (Patients developing any medical condition that interferes with the outcomes after enrolment in the study will be excluded).

Where it's running

  • Suez Canal University
    Ismailia, Egypt
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.