Evaluating the need of nasal splint in septoplasty surgeries
Not Applicable
- Conditions
- septoplasty.Deflection or deviation of septum (nasal)(acquired)
- Registration Number
- IRCT2017021832645N1
- Lead Sponsor
- Tabriz university of medical sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 48
Inclusion Criteria
inclusion:
1-consent to participate in the study
2-septoplasty candidates
exclusion:
1-Lack of consent to participate in the study
2-Patients which need additional surgeries while undergoing septoplasty surgery
3-Patients that won't cooperate during follow-up period
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Complications. Timepoint: 2 weeks after intervention. Method of measurement: clinical examination.
- Secondary Outcome Measures
Name Time Method Pain severity assessmnet. Timepoint: 2 weeks after intervention. Method of measurement: visual pain scale.