Condition 1: septorhinoplasty. Condition 2: Periorbital Ecchymosis. Condition 3: Periorbital Edema.
Conditions
Interventions
Intervention 1: Intervention group: People who are seeking primary nasal surgery for aesthetic or functional improvement of breathing and who have visited Taleghani Hospital between 1404 and 1405 and
Sponsors
Shahid Beheshti University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to 50 Years
Inclusion criteria
Inclusion criteria: Adult patients aged 18 to 50 years who are selected for primary open rhinoplasty. Patient has no previous rhinoplasty or septoplasty history. Willing to participate in the study and comply with follow-up requirements. All individuals with their own septal graft undergo routine septorhinoplasty. Patient has no nasal polyps or perforated septum.
Exclusion criteria
Exclusion criteria: Reluctance to participate or continue to participate in the study Any need to perform non-routine surgical techniques during the operation, depending on the patient's clinical condition Self-initiation of any medication that could affect swelling or bruising or subconjunctival hemorrhage or nasal mucosal rupture after surgery.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Periorbital Ecchymosis. Timepoint: 3 and 7 days after surgery. Method of measurement: Using the scale first proposed by Kara and Gökalan in 1999.;Subconjunctival hemorrhage. Timepoint: 3 and 7 days after surgery. Method of measurement: Using the scale first proposed by Kara and Gökalan in 1999.;Periorbital Edema. Timepoint: 3 and 7 days after surgery. Method of measurement: Using the scale first proposed by Kara and Gökalan in 1999.;Intranasal Mucosal Injury. Timepoint: 3 and 7 days after surgery. Method of measurement: Using the scale first proposed by Mori et al. in 2008. | — |
Secondary
| Measure | Time frame |
|---|---|
| Comparison of the severity of post-operative periorbital Ecchymosis between the intervention and control groups. Timepoint: After the end of sampling. Method of measurement: Using a scale first proposed by Kara and Gökalan in 1999.;Comparison of the severity of post-operative periorbital Edema between the intervention and control groups. Timepoint: After the end of sampling. Method of measurement: Using a scale first proposed by Kara and Gökalan in 1999.;Comparison of the severity of post-operative subconjunctival hemorrhage between the intervention and control groups. Timepoint: After the end of sampling. Method of measurement: Using a scale first proposed by Kara and Gökalan in 1999.;Comparison of the severity of post-operative Intranasal Mucosal Injury between the intervention and control groups. Timepoint: After the end of sampling. Method of measurement: Using a scale first proposed by Mori et al. in 2008. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAref Zarei
Shahid Beheshti University of Medical Sciences
Outcome results
None listed