Echymosis and Edema. Surgical instruments, materials and general- and plastic-surgery devices (including sutures) associated with adverse incidents
Conditions
Interventions
Intervention 1: Intervention group: The intervention group includes one side of the nose in patients who have undergone open rhinoplasty surgery and after surgery will receive asparagus seeds as a gel
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All candidates for rhinoplasty Informed consent to participate in the study
Exclusion criteria
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactFeizollah Niazi
Shahid Beheshti University of Medical Sciences
Outcome results
None listed