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Effect of Airway Integrated Nasal Packing With Different Material

Comparison of Nasal Packing Methods:Nasal Packing Was Done With Nasopore@, Airway-integrated Nasopore@ and Airway-integrated Vaseline Gauze

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01562691
Enrollment
60
Registered
2012-03-26
Start date
2009-06-30
Completion date
2011-12-31
Last updated
2012-03-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Postoperative., Postoperative Respiratory Complications

Keywords

nasal packing, nasal airway, septoplasty, oxygen saturation, postoperative pain

Brief summary

The purpose of this study is to determine the effect of integrated airway in nasal packing material foe patients receiving nasal septoplasty surgery.

Detailed description

Nasal packing with integrated airway had been claimed to improve body oxygenation following septal surgery. This randomized control study examined the effect of airway integrated with nasal packing, in terms of its improvement on oxygen saturation. Sixty patients with septal deviation and hypertrophic turbinate were randomized into three groups. Group 1 patients were packed with only nasopore@ after surgery. Nasopore@ with integrated airway was used for group 2 patients; and Vaseline gauze integrated with airway for group 3 patients. Hemodynamic parameters were sequentially checked. Nasal pain sensation was recorded using visual analog scale.

Interventions

PROCEDURENasopore

Bilateral nasal packing using Nasopore without airway integrated

PROCEDUREairway integrated Nasopore

post nasoseptoplasty with nasal packing using airway integrated Nasopore

PROCEDUREairway-integrated Vaseline gauze

post nasal septoplasty with packing using airway-integrated Vaseline gauze

Sponsors

Chi Mei Medical Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* patients who underwent septoplasty for septal deviation and chronic hypertrophic rhinitis

Exclusion criteria

* patients with comorbidities of coronary heart disease, arrhythmia, chronic obstructive lung diseases, and with past history of any nasal surgery were excluded.

Design outcomes

Primary

MeasureTime frameDescription
change of the SpO2 from baseline to 48 hours post-operationrecords of the SpO2 at 48 hours post-operationrecords of the SpO2 at 48 hours post-operation
change of the SpO2 from baseline to 6 hours post-operationrecords of the SpO2 at 6 hours post-operationrecords of the SpO2 at 6 hours post-operation
change of the SpO2 from baseline to 12 hours post-operationrecords of the SpO2 at 12 hours post-operationrecords of the SpO2 at 12 hours post-operation
change of the SpO2 from baseline to 18 hours post-operationrecords of the SpO2 at 18 hours post-operationrecords of the SpO2 at 18 hours post-operation
oxyhemoglobin saturation by pulse oximetry, SpO2SpO2 was measured 30 minutes before operation,SpO2 was measured 30 minutes before operation using O2 saturation monitor.
change of SpO2 from baseline to 4 hours post-operationrecords of the SpO2 at 4 hours post-operationrecords of the SpO2 at 4 hours post-operation

Secondary

MeasureTime frameDescription
change of postoperation pain scale from baseline to 4 hours post-operationrecord of postoperation pain scale at 4 hours post-operationrecord of postoperation pain scale at 4 hours post-operation
change of postoperation pain scale from baseline to 6 hours post-operationRecord of postoperation pain scale at 6 hours post-operationrecord of postoperation pain scale at 6 hours post-operation
postoperation painrecord of postoperation pain scale at 2 hous post operationrecord of postoperation pain scale at 2 hours post-operation

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026