Spreader Graft and Lateral Crural Overlay Technique in Rhinoplasty

NCT ID: NCT01852643

Last Updated: 2013-05-14

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

COMPLETED

Clinical Phase

PHASE2/PHASE3

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-02-29

Study Completion Date

2012-12-31

Brief Summary

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Most of the studies performed to compare the present techniques of rhinoplasty have been based on the clinical examination and change of postoperative complaints that cannot be very precise in evaluating the advantages of one technique over another. Therefore, in this study the investigators are going to compare the efficacy of spreader graft and lateral crural overlay techniques by an objective method, rhinomanometry.

Detailed Description

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Conditions

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Rhinoplasty Techniques

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Spreader graft

Group Type ACTIVE_COMPARATOR

Spreader graft

Intervention Type PROCEDURE

Spreader graft technique is performed by a group of expert surgeons.

Lateral crural overlay

Group Type ACTIVE_COMPARATOR

Lateral crural overlay

Intervention Type PROCEDURE

Lateral crural overlay technique is performed by a group of expert surgeons.

Interventions

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Spreader graft

Spreader graft technique is performed by a group of expert surgeons.

Intervention Type PROCEDURE

Lateral crural overlay

Lateral crural overlay technique is performed by a group of expert surgeons.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Candidates of rhinoplasty
* Willingness to participate

Exclusion Criteria

* Having structural problems such as nasal obstruction
* History of the deformity requiring rhinoplasty of the deviated septum
* Hardening surgery
* New clinical conditions or a change in therapeutic technique
* Unwillingness to continue participating in the study
* Having no access to subjects after the operation
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Isfahan University of Medical Sciences

OTHER

Sponsor Role lead

Responsible Party

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Dr. Amiryousef Ahmadnia

Dr.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Amiryousef Ahmadnia, MD

Role: PRINCIPAL_INVESTIGATOR

Isfahan University of Medical Sciences

Locations

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Department of Plastic Surgery, Alzahra Hospital

Isfahan, Isfahan, Iran

Site Status

Countries

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Iran

Other Identifiers

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390548

Identifier Type: -

Identifier Source: org_study_id

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