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Completed

NCT Number: NCT00467714

Evaluation Of Cloumella Strut Effect In Tip Rotation

The role of strut in rhinoplasty has been debated for many years and many research has been made over this problem but there is no significant data for descision of surgeon, so this study was designed to evaluate the effect of columellar strut in tip projection and rotation.

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Key information

Conditions

Nose Deformities, Acquired Nose Diseases Otorhinolaryngologic Diseases Respiratory Tract Diseases

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Imam Hospital

Tehran, Tehran Province, 19799, Iran

About this study

In selected case of rhinoplasty use strut randomly and blindly evalute the effect of it in tip rotation and projection.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • RHINOPLASTIC PATIENTS

Exclusion criteria

  • REVISION SURGERY,
  • INCOMPLETE STRIP,
  • FACIAL ANOMALY

Treatment and study plan

Rhinoplasty

Procedure

COLUMELLA STRUT PLACEMENT

Other names: no other name

Primary outcomes

  1. TIP ROTATION

    Time frame: 6 month after surgery

Secondary outcomes

  1. TIP PROJECTION

    Time frame: 6 month after surgery

Sponsors and collaborators

Lead sponsor

Tehran University of Medical Sciences

Other

Registry information

Official study title

Evaluation of Cloumella Strut in Maintenance of Tip Rotation

Important dates

Study start
2007
Primary completion
2008
Study completion
2008
First posted
May 1, 2007
Registry last updated
Nov 18, 2008

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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