Management of nasotrancheal intubation complications

Phase 2

• Conditions: Endotracheal nasal tube bacterial load.; Lung diseases due to external agents; J60-J70

• Registration Number: IRCT2016102122951N2
• Lead Sponsor: Research deputy of Tabriz University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 44

Inclusion Criteria

All patients who are going to have maxillofacial surgery and nasotracheal intubation; age from 20 to 60 years
Exclusion criteria: contraindications of nasotracheal intubation; nasal polyps; Chronic sinusitis; upper airway infections; allergy to mupirocin; pregnancy and lactation.

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Endotracheal nasal tube bacterial load. Timepoint: after surgery. Method of measurement: Microbial culture.;Nasal congestion. Timepoint: 0, 2, 4, 6, 12 hours After anesthesia. Method of measurement: questionnaire.;Facilitate breathing through the nose. Timepoint: 0, 2, 4, 6, 12 hours After anesthesia. Method of measurement: questionnaire.;Ease of extubation. Timepoint: After anesthesia. Method of measurement: check list.