Nasal congestion.
Conditions
Interventions
Intervention 1: Patients will be randomly assigned to the intervention group (Mometasone Nasonex = Mometasone Furoate 0.05%, Organon). After surgery, each drug will be sprayed three times a day for 3
Sponsors
Mashhad University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Maxillary orthognathic surgery Absence of sinus and allergic disease Absence of craniofacial syndromes and cleft lip and palate Absence of sinus medication
Exclusion criteria
Exclusion criteria: Patient's unwillingness to participate in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Average score of the standard SNOT 20 (sino-nasal outcome test) questionnaire. Timepoint: On the third and tenth day after surgery. Method of measurement: The standard SNOT 20 (sino-nasal outcome test) questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactAlireza Ebrahimpour
Mashhad University of Medical Sciences
Outcome results
None listed