Bronchoscopy Clinical Trial
Official title:
Effect of Xylometazoline Administration During Nasal Flexible Bronchoscopy: A Double Blind, Randomized, Placebo-controlled Trial
Flexible bronchoscopy is a commonly performed procedure and is usually performed transnasally. The optimal topical anesthesia regimen for bronchoscopy is investigational. Topical Vasoconstrictors like xylometazoline produce decongestion of nasal mucosa and may make insertion of bronchoscope easier. The addition of topical vasoconstrictor to lignocaine may have advantage in terms of patient comfort and for reducing local complications. Although evaluated in the settings of nasal endoscopy and nasotracheal intubation, randomized trials on the role of topical vasoconstrictors during flexible bronchoscopy are not available. The aim of this randomized trial is to study the effect of topical nasal xylometazoline administration during flexible bronchoscopy.
Study design: Randomized double-blind placebo controlled study Study setting: Bronchoscopy
room in Department of pulmonary medicine and sleep disorders at AIIMS, New Delhi Sample size:
200 patients (100 in each arm)
Inclusion criteria:
a) All adults > 18 years of age undergoing flexible bronchoscopy via nasal route
Exclusion criteria:
1. Uncontrolled hypertension
2. coronary artery disease
b) Pregnancy c) refusal of consent d) Hypoxemia (oxygen saturation [by pulse oximetry] < 92%
with Fio2 of ≥ 0.3 e) Bronchoscopy not performed by nasal route f) Bronchoscopy performed
through an artificial airway
Randomisation:
Computer generated Block randomisation with block size of 10 will be used to generate list of
random numbers based on which subjects will be allocated to either of the groups.
Procedure of study The operator, assistant, drug administrator and outcomes assessor will be
blinded. Patients meeting eligibility criteria will be randomized to receive either study
drug Xylometazoline (0.1% nasal drops) (Otrivin, Novartis) (3 drops into each nostril) or
0.9% saline (3 drops into each nostril) placebo. This will be administered as ten minutes
before bronchoscopy. This will be followed by the standard topical anesthesia procedure
followed in our institution involving 5ml of 2% lignocaine gel into the nostril and 4 sprays
of 10% lignocaine to the pharynx. Nebulized lignocaine shall not be administered. Transnasal
flexible bronchoscopy will be performed with additional 1% lignocaine solution administered
as "spray as you go" method. All diagnostic procedures or airway inspection procedures will
be included. Patients shall undergo hemodynamic monitoring throughout the procedure.
Procedures shall be performed without administration of upfront sedation and intraprocedural
sedation shall be at the discretion of the operator.
Data will be recorded on a predesigned proforma. Baseline patient characteristics will be
compared between the two groups. Categorical variables will be summarised by frequency (%)
and chi-square test of proportion will be used to compare between the two groups.Quantitative
variables will be summarised by mean±SD or median(IQR),as appropriate. Student's t-test or
Wilcoxon rank sum test as appropriately be used to compare distribution of quantitative
variables between the two groups. Stata statistical software will be used for data analysis.
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