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NCT06291402 Clinical Trial

Nasal Packing Duration and Development of Pharyngitis After Septorhinoplasty Surgery

Rhinitis Clinical Trial

Official title:
Nasal Packing Duration and Its Role in the Development of Pharyngitis After Septorhinoplasty Surgery: A Prospective Observational Study

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT06291402
Other study ID # RC 34-1-2024
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 10, 2024
Est. completion date June 15, 2024

Study information
Verified date April 2024
Source Al-Azhar University
Contact Neveen Kohaf, Ph.D
Phone +201060383012
Email nevenabdo@azhar.edu.eg
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Septoplasty or septal reconstruction is a corrective surgical procedure performed to straighten the nasal septum. It may be associated with numerous complications. To minimize these complications, both nasal cavities are frequently packed with different types of nasal packing. In our study we will try to find relationship between duration of nasal packing and postrhinoplasty sore throat and pharyngitis.

Description:

Nasal packing affects swallowing by different mechanisms. It may affect swallowing as a result of nasal congestion, constant mouth breathing, throat dryness and pharyngitis. Postoperative sore throat causes patient dissatisfaction and poor pain control. Several interventions could be performed to reduce sore throat and pharyngitis and increase patient satisfaction , which may not be convenient for all patients, such as gargling or sprays

Recruitment information / eligibility
Status Recruiting
Enrollment 100
Est. completion date June 15, 2024
Est. primary completion date June 15, 2024
Accepts healthy volunteers No
Gender All
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - ASA I and II patients - aged from 20 to 40 years old - undergo septorhinoplasty Exclusion Criteria: - Bleeding disorders - Uncontrolled hypertension - Cardiovascular diseases - Uncontrolled diabetes mellitus - Collagen disorders - Pregnancy

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Egypt Neveen Kohaf Tanta

Sponsors (2)
Lead Sponsor Collaborator
Al-Azhar University Benha University

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Sore throat The incidence of Sore throat will be graded as 0 = Nil, 1 = Mild, 2 = Moderate and 3 = Severe as possible. 48 hours postoperatively
Secondary Dysphagia The incidence of Dysphagia will be recorded 48 hours postoperatively
Secondary Throat irritation The incidence of throat irritation will be recorded 48 hours postoperatively
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