Dental implant. Presence of tooth-root and mandibular implants
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Implant candidate patients in the area of extracted teeth At least 18 years old No systemic problems
Exclusion criteria
Exclusion criteria: Smokers with more than 10 cigarettes per day Patients with allergies to any of the substances used in this study Patients undergoing head or neck radiation therapy or chemotherapy in the 12 months prior to surgery Pregnant or lactating patients
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes in mesiodistal (MD) and vestibulo-palatal/lingual (VP/L) dimensions. Timepoint: 2 months after the operation. Method of measurement: The maximum diameter of the socket is measured using the William probe and recorded in both the mesiodistal and vestibulo-lingual/palatal dimensions at the crestal level.;The amount of pain. Timepoint: During 7 days after the operation. Method of measurement: Visual Analogue Scale.;Soft tissue quality. Timepoint: 7 days after extraction. Method of measurement: The quality of the soft tissue of the surgical area (tissue color, tissue consistency, pus secretion, bleeding) will be evaluated through a modified version of Landry, Turnbull and Howley's Healing Index (HI). | — |
Secondary
| Measure | Time frame |
|---|---|
| Histomorphological factors. Timepoint: After 2 months. Method of measurement: A sample will be taken from Saket for histological evaluation. After fixation and decalcification, the samples will be stained with hematoxylin and eosin (H&E) and histomorphological factors (percentage of remaining scaffold, bone and connective tissue) will be evaluated. | — |
Countries
Iran (Islamic Republic of)
Contacts
Tabriz University of Medical Sciences