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Non Grafted Maxillary Sinus Floor Elevation With Implant Placement Versus the Use of Short Endosseous Implants

Sponsor
Cairo University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03661957
Collaborator
(none)
10
Enrollment
1
Location
2
Arms
7
Anticipated Duration (Months)
1.4
Patients Per Site Per Month

Study Details

Study Description

Brief Summary

Assessment the need for sinus floor elevation when restoring atrophic posterior maxilla or it will be enough to use of short implant

Condition or Disease Intervention/Treatment Phase
  • Procedure: Non grafted maxillary sinus floor elevation with simultaneous implant placement
  • Procedure: using short dental implants for posterior atrophic maxilla
 N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Non Grafted Maxillary Sinus Floor Elevation With Simultaneous Implant Placement Versus the Use of Short Endosseous Implants
Anticipated Study Start Date :
Sep 1, 2018
Anticipated Primary Completion Date :
Dec 1, 2018
Anticipated Study Completion Date :
Apr 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Non grafted maxillary sinus floor elevation with implant pacem

Procedure: Non grafted maxillary sinus floor elevation with simultaneous implant placement
lateral window for sinus elevation ,membrane elevation ,implant placement , membrane for window closure
Experimental: using short dental implants for posterior atrophic maxilla

Procedure: using short dental implants for posterior atrophic maxilla
placement of short dental implant with bone height below 8mm

Outcome Measures

Primary Outcome Measures

  1. primary stability [6 months]

    measuring primary stability using osstel

Secondary Outcome Measures

  1. marginal bone loss [6 months]

    measuring marginal bone loss using cone beam ct

Eligibility Criteria

Criteria

Ages Eligible for Study:
25 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

  • Immunodeficiency pathology, bruxism, stress situation (socially or professionally), emotional instability, and unrealistic aesthetic demands.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ahmed Maher Mansour Cairo Egypt

Sponsors and Collaborators

  • Cairo University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ahmed Maher Mansour, dentist-master student, Cairo University
ClinicalTrials.gov Identifier:
NCT03661957
Other Study ID Numbers:
  • cairo university 99
First Posted:
Sep 7, 2018
Last Update Posted:
Sep 7, 2018
Last Verified:
Sep 1, 2018
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No

Study Results

No Results Posted as of Sep 7, 2018