Comparison of two Methods of Rhinoplasty

Phase 2

• Conditions: Rhinoplasty.; Complications of medical and surgical care; Y40, Y41,

• Registration Number: IRCT2015081123594N1
• Lead Sponsor: Vice chancellor for research, Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 80

Inclusion Criteria

This study will be conducted on 80 volunteer eligible cases for rhinoplasty. All enrolled cases are white and from the same ethnic group. The exclusion criteriais known bleeding or coagulation disorder

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Amount of intra-operational bleeding. Timepoint: During surgery. Method of measurement: Intraoperative bleeding volumes will be measured in separate suction bottles for each side.;Edema. Timepoint: After surgery. Method of measurement: Postoperative edema will be assessed by the ward residents unaware of operation variations.;Ecchymosis. Timepoint: After surgery. Method of measurement: Ecchymosis will be assessed by the ward residents unaware of operation variations.

Secondary Outcome Measures

Name	Time	Method
o. Timepoint: No. Method of measurement: No.