Clinical Trials Logo

Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03732885
Other study ID # NCT035
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date November 1, 2018
Est. completion date July 15, 2019

Study information

Verified date November 2018
Source Cairo University
Contact Sohaib M Elsheikh, masters
Phone 00201222500517
Email alzamzamy44@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

To investigate the efficacy of osseodensification drills (Densah bure) as a new closed sinus lift tool and to compare the effect of it in bone gaine versus traditional osteotomes.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 24
Est. completion date July 15, 2019
Est. primary completion date April 15, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 25 Years to 55 Years
Eligibility Inclusion Criteria:

- Patients with partially edentulous in the posterior area of the maxilla, with a residual ridge that allowed insertion of =8 mm length implants.

- both sexes.

- No intraoral soft and hard tissue pathology

- No systemic condition that contraindicate implant placement.

Exclusion Criteria:

- Sinus pathology.

- Heavy smokers more than 20 cigarettes per day.

- Patients with systemic disease that may affect normal healing.

- Psychiatric problems.

- Disorders to implant are related to history of radiation therapy to the head and neck neoplasia, or bone augmentation to implant site.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
densah burs osseo densification drills
maxillary sinus floor elevation during implant placement using Densah burs
Summer's Osteotomes
maxillary sinus floor elevation during implant placement using Summer's Osteotomes

Locations

Country Name City State
Egypt Sohaib M Elsheikh Cairo

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary implant stability measurement of implant stability using the Ostell 6 months after surgery
Secondary bone gain measurement of bone gain around implant using cone-beam computed tomography CBCT 6 months after surgery
See also
  Status Clinical Trial Phase
Completed NCT04160689 - Influence of the Implant Connection on Facial Tissues Maturation Phase 4
Completed NCT04139512 - One-abutment One-time for Immediate Restoration Procedure in the Esthetic Zone Phase 4
Active, not recruiting NCT04421066 - Histological, Genetic and Epigenetic Analysis of Procedures Related With Dental Implants
Completed NCT04054271 - Effects of ABO Blood Types on the Survival and Marginal Bone Resorption of Dental Implants
Completed NCT04679922 - Fascia Lata Allograft Versus Subepithelial Connective Tissue Grafts in the Peri-Implant Mucosal Thickness Enhancement. N/A
Recruiting NCT06206499 - Laterally Rotated Flap for Soft Tissue Augmentation Around Maxillary Loaded Osseointegrated Dental Implant N/A