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evaluation of vertical bone augmentation by tenting abutment regarding usage of sticky bone in comparison with xenograft in posterior ridge of mandible : a clinical trial

evaluation of vertical bone augmentation by tenting abutment regarding usage of sticky bone in comparison with xenograft in posterior ridge of mandible : a clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20130813014350N6
Enrollment
10
Registered
2024-10-17
Start date
2025-03-21
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

alveolar ridge defect. Loss of teeth due to accident, extraction or local periodontal disease

Interventions

Intervention 1: the intervention group: to prepare i-PRF, 10 ml of the patients venous blood is centrifuged in a test tube without anticoagulant for 3 minutes at a speed of 700 rpm. i-PRF (the orange-

Sponsors

Vice President of Research and Technology of Gilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients with complete edentulism or bilateral posterior part of the mandible 2) Patients with index plaque before surgery less than 20%

Exclusion criteria

Exclusion criteria: 1) People with blood diseases or uncontrolled diabetes 2) Smokers 3) Pregnant and lactating women 4) People with a history of radiation therapy or chemotherapy or treatment with bisphosphonate 5) Patient with untreated periodontitis

Design outcomes

Primary

MeasureTime frame
Comparison of the vertical height of the posterior ridge of the mandible before and 6 months after reconstruction using xenograft and tenting abutment and using sticky bone and tenting abutment in millimeters. Timepoint: Comparison of the vertical height of the posterior ridge of the mandible before and 6 months after reconstruction using xenograft and tenting abutment and using sticky bone and tenting abutment in millimeters after 6 months. Method of measurement: Cone Beam Computed Tomography.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactBardia Vadiati Saberi

Guilan University of Medical Sciences

dr.bardia_vad@yahoo.com+98 13 3348 6407

Outcome results

None listed

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