Non-grafted Maxillary Sinus Floor Elevation With Simultaneous Implant Placement Using Different Implant Lengths

NCT ID: NCT03731650

Last Updated: 2018-11-06

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

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-01-01

Study Completion Date

2019-08-15

Brief Summary

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twenty recruited patients indicated for sinus augmentation and simultaneous implant placement will be divided into two groups (10 in each of the groups).to evaluate \& compare bone formation \& implant stability after shneiderian membrane elevation and augmentation with graft less tenting technique with different implant lengths.

group one will receive 8mm implant lenght while group two will receive 10mm implants.

Detailed Description

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Conditions

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Maxillary Sinus Lift

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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active comparator

Group Type EXPERIMENTAL

maxillary sinus lift

Intervention Type PROCEDURE

non grafted maxillary sinus floor augmentation with simultaneous implant placement

placebo

Group Type EXPERIMENTAL

maxillary sinus lift

Intervention Type PROCEDURE

non grafted maxillary sinus floor augmentation with simultaneous implant placement

Interventions

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maxillary sinus lift

non grafted maxillary sinus floor augmentation with simultaneous implant placement

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* patient with atrophic maxilla \& pneumatized maxillary sinus with residual bone height at least 4mm of residual ridge
* both sexes

Exclusion Criteria

* patients with systematic diseases that may affect normal healing
* sinus pathology
* heavy smokers more than 20 cigarettes per day
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Cairo University

OTHER

Sponsor Role lead

Responsible Party

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Ahmed Abdulnasser

principal investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Central Contacts

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ahmed abdul nasser ali, BDS

Role: CONTACT

00201115905965

ahmed abdel rahman mohammed, MDS

Role: CONTACT

00201005261204

Other Identifiers

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aaali.cairo university

Identifier Type: -

Identifier Source: org_study_id

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