Bone resorption in the maxilla.
Conditions
Interventions
Intervention 1: Second Intervention group: Self-assembling peptide nanofiber (the company-made) is placed in a single dose (1 ml) to repair the sinus cavity and is tested for 6 months. Intervention 2:
Sponsors
Iran University of Medical Sciences
Knowledge enterprise company “Tavakol Pars Biomimetic Technologies Company
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: Patient will require sinus augmentation bone height between alveolar crest and maxillary sinus less than 8 millimetres. Patient has good oral and dental hygiene Do not have maxillary sinus diseases
Exclusion criteria
Exclusion criteria: Smoking Pregnancy and lactation Uncontrolled diabetes Alcohol consumption Autoimmune diseases Cancer and undergoing chemotherapy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: The fourteenth day. Method of measurement: McGill Pain Questionnaire (MPQ).;Wound healing. Timepoint: The fourteenth day. Method of measurement: Using dental tweezers by examining alveolar osteitis based on BLUM'S criteria.;The amount of vertical height. Timepoint: Baseline and after 6 months. Method of measurement: CBCT.;Implant stability. Timepoint: After 6 months. Method of measurement: OSTELL.;Bone tissue quality. Timepoint: Post-implantation. Method of measurement: Tissue staining. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactShima Tavakol
Iran University of Medical Sciences
Outcome results
None listed