Comparison of septoplasty with and without nasal packing on the complications and outcomes of surgery in patients who are candidate for septoplasty

Not Applicable

• Conditions: Condition 1: Pain. Condition 2: Anxiety.; Other acute postprocedural pain; Anxiety disorder, unspecified; G89.18

• Registration Number: IRCT20120215009014N243
• Lead Sponsor: Hamedan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 14 January 2019

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 56

Inclusion Criteria

Age of 18 to 65 years;
Candidate for septoplasty

Exclusion Criteria

Incidence of trauma after surgery;
A history of nasal granulomatosis;
Need for turbinate surgery

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Measuring pain. Timepoint: 24 hours, one week, and 3 months after surgery. Method of measurement: Using Visual Analog Scale (VAS).;Measuring anxiety. Timepoint: 24 hours, one week, and 3 months after surgery. Method of measurement: Usng standard questionnaire.;Assessing quality of breathing and sleep. Timepoint: 24 hours, one week, and 3 months after surgery. Method of measurement: Through history taking.

Secondary Outcome Measures

Name	Time	Method
Measuring the severity of bleeding and leakage. Timepoint: 24 hours and one week after surgery. Method of measurement: Through physical examination.;Measuring the septal hematoma. Timepoint: 24 hours and one week after surgery. Method of measurement: Through physical examination.