: Evaluation of the effectiveness of plantago ovata on ecchymosis and edema afterrhinoplasty

Phase 3

Recruiting

• Conditions: Echymosis and Edema.; Surgical instruments, materials and general- and plastic-surgery devices (including sutures) associated with adverse incidents; Y81.3

• Registration Number: IRCT20200523047549N2
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 30 May 2022

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 33

Inclusion Criteria

All candidates for rhinoplasty
Informed consent to participate in the study

Exclusion Criteria

Pregnancy of patients
Heart and lung diseases
People with a history of previous rhinoplasty
Use of other local or oral medications for edema and ecchymosis

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Severity of edema. Timepoint: 8 hours after surgery, 16 hours after surgery, 24 hours and 48 hours after rhinoplasty. Method of measurement: Physical and clinical evaluation based on Pitting Edema criteria.;Severity of ecchymosis. Timepoint: 8 hours after surgery, 16 hours after surgery, 24 hours and 48 hours after rhinoplasty. Method of measurement: Physical and clinical evaluation.