Status:
COMPLETED
Topical Lidocaine Anesthesia for Nasopharyngeal Sampling
Lead Sponsor:
Ataturk University
Conditions:
Nasopharyngeal Sampling
Local Anesthesia
Eligibility:
All Genders
18-65 years
Phase:
NA
Brief Summary
Introduction: Nasopharyngeal sampling is widely used in the diagnosis of the Coronavirus Disease 2019 (COVID-19). The aim of this study is to evaluate the effects of topical lidocaine application for ...
Detailed Description
This study is a prospective randomized placebo-controlled study with restricted randomization of an allocation ratio of 1:1. We used Random Allocation Software (RAS) for randomization. The study is co...
Eligibility Criteria
Inclusion
- \-
- The inclusion criteria of the study is:
- being 18 years and older
- volunteering to participate in the study.
Exclusion
- The exclusion criteria of the study is:
- taking analgesic drugs before admission,
- pregnancy,
- lactation,
- having a bleeding disorder, \*known allergy to Lidocaine, \* previous nasal trauma or operation,
- having respiratory tract infection symptoms (such as fever, headache, runny nose, sore throat, cough, sneeze, breathlessness),
- having a chronic disease (diabetes, cancer, heart disease, asthma, COPD, etc.).
Key Trial Info
Start Date :
September 1 2020
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 30 2020
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT04885777
Start Date
September 1 2020
End Date
October 30 2020
Last Update
May 18 2021
Active Locations (1)
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1
Ataturk University
Erzurum, Turkey (Türkiye)