Clinical Evaluation of Stability of Dental Implant Placed Simultaneously With Closed Sinus Lifting Using Hydraulic Lift Technique Versus Summer's Osteotome Technique in Posterior Edentulous Maxilla (RCT)

NCT ID: NCT04659720

Last Updated: 2020-12-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-10-27

Study Completion Date

2021-11-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

Clinical evaluation of stability of dental implant placed simultaneously with closed sinus lifting using hydraulic lift technique versus summer's osteotome technique in posterior edentulous maxilla (RCT)

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Clinical evaluation of stability of dental implant placed simultaneously with closed sinus lifting using hydraulic lift technique versus summer's osteotome technique in posterior edentulous maxilla (Randomised clinical trial)

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Evaluations, Diagnostic Self

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

summers' osteotome technique for closed sinus lift

Implant stability will be evaluated after closed sinus lift using summer's osteotome technique in posterior edentulous maxilla

Group Type ACTIVE_COMPARATOR

Hydrolic lifter device

Intervention Type DEVICE

evaluation of implant stability after closed sinus lifting by hydraulic lift technique using hydraulic lifter device

Patient satisfaction evaluation after closed sinus lifting using summers' osteotome technique

* Will be assessed numerically using a patient satisfaction chart .
* Time of assessment: immediately after surgery

Group Type ACTIVE_COMPARATOR

Patient satisfaction evalution using hydraulic lifter device

Intervention Type BEHAVIORAL

patients satisfaction will be evaluated numerically after using hydraulic lift technique by hydraulic lifter device for closed sinus lifting in posterior edentulous maxilla

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Hydrolic lifter device

evaluation of implant stability after closed sinus lifting by hydraulic lift technique using hydraulic lifter device

Intervention Type DEVICE

Patient satisfaction evalution using hydraulic lifter device

patients satisfaction will be evaluated numerically after using hydraulic lift technique by hydraulic lifter device for closed sinus lifting in posterior edentulous maxilla

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Edentulous patients in the maxillary posterior region.
* Patients in need to fixed restorations in posterior region.
* Patients with healthy systemic conditions. (Apparently medically free)
* Patients with adequate inter-arch space for placement of the prosthetic part of the implant .
* Patients who had approximately 5-8 mm of available bone height between crest of bone and floor of sinus
* Both sexes.
* Patients with Good oral hygiene
* Patients more than 20 years old
* Cooperative and motivated patients

Exclusion Criteria

* Patients with local pathological defects related to posterior maxilla.
* Heavy smokers.
* Abnormal habits that may alter results such as alcoholism or parafunctional habits.
* Patients with systemic diseases that may affect normal healing.
* Patients with psychiatric problem
* Patients with history of recent radiation therapy to the head and neck area.
* Patients with aggressive periodontitis.
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Cairo University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Hassan Mohammad

Assoc.professor in maxillo facial surgery

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Hassan Abdelghany, PHD

Role: PRINCIPAL_INVESTIGATOR

Assoc.professor

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Cairo university

Cairo, , Egypt

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Egypt

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

131020

Identifier Type: -

Identifier Source: org_study_id