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The effect of the remaining bony walls of the maxillary sinus on the quality of the formed bone in dental implants

A clinical trial to investigate the effect of the remaining bony walls of the maxillary sinus on the quality of the formed bone in single maxillary posterior teeth implants, compared to multiple maxillary posterior teeth implants after sinus lift

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210204050239N1
Enrollment
40
Registered
2021-02-07
Start date
2021-03-21
Completion date
Unknown
Last updated
2021-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Teeth implants. Presence of other specified functional implants

Interventions

Intervention 1: Intervention group: Intervention group I will receive sinus lift surgery for single posterior maxillary implants with a residual alveolar bone thickness of 2-4 mm and 5 bony walls (med

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 50 Years

Inclusion criteria

Inclusion criteria: Aged range of 20-50 years Patients candidate for maxillary posterior teeth implants with a minimum of 2-4 mm alveolar bone thickness according to CBCT with a need for the sinus lift

Exclusion criteria

Exclusion criteria: The presence of systemic diseases Patients who cannot undergo routine oral surgery Patients who smoke more than 10 cigarettes daily The presence of sinusitis Pregnant and breastfeeding women History of allergies Membrane perforations more than 2 mm

Design outcomes

Primary

MeasureTime frame
The bone mineral density formed. Timepoint: 6 months after the intervention. Method of measurement: Cone beam computed tomography.;The rate of angiogenesis. Timepoint: 6 months after the intervention. Method of measurement: Histological osteogenesis with hematoxylin-eosin staining.;Number of osteoblasts per unit area. Timepoint: 6 months after the intervention. Method of measurement: Histological osteogenesis with hematoxylin-eosin staining.

Secondary

MeasureTime frame
Implant stability in the bone graft. Timepoint: Immediately and 4 months after the intervention. Method of measurement: Osstell Mentor.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehran Farhadi

Mashhad University of Medical Sciences

Mehran.farhaadi74@gmail.com+98 51 3883 2300

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026