NCT06563050Not yet recruiting
Comparison Between Different Ways for Using Lidocaine During FB
Comparison Between Nebulized Lidocaine, Lidocaine Spray, or Their Combination for Topical Anesthesia During Diagnostic Flexible Bronchoscopy: a Randomized Trial
Source: ClinicalTrials.gov · Last updated 22 Aug 2024 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
compare the efficacy and safety of nebulized lidocaine, oropharyngeal lidocaine spray, or their combination for better outcome of topical anesthesia in subjects undergoing diagnostic FB; severity of cough , pain during procedure , cumulative dose of anesthesia needed and its adverse reaction , overall satisfaction .
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 240 (estimated)
- First submitted
- 5 Aug 2024
- Start date
- Sept 2024
- Primary completion date
- Sept 2026
- Lead sponsor
- Assiut University
- Diseases
- Lung cancer
- NCT number
- NCT06563050
What you commit to
- Study type: Interventional
- Planned participants: 240
- From Sept 2024 to the primary completion date, Sept 2026
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- known hypersensitivity to lidocaine.
- failure to provide informed consent.
Other
- Pregnancy.
- hemodynamic instability.
Who the study is looking for
- Patients above 18 years old will undergo FB are included in this study.
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.