Trials / Terminated
TerminatedNCT03829618
Lidocaine Administration During Flexible Bronchoscopy and Endobronchial Ultrasound
- Status
- Terminated
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 29 (actual)
- Sponsor
- Milton S. Hershey Medical Center · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to assess if there is decrease in cough during flexible bronchoscopy and endobronchial ultrasound when different modes of lidocaine administration are used. The modes of administration being evaluated are topical, nebulized and atomized.
Conditions
- Bronchiectasis Adult
- Mediastinal Lymphadenopathy
- Pneumonia
- Chest--Diseases
- Infiltrates
- Bronchopulmonary Disease
- Cancer, Lung
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Topical lidocaine | 1% lidocaine topically applied in 4 mL aliquots |
| DRUG | Nebuliser solution | 2% lidocaine dose at 2 mg/kg (max 160 mg) applied via jet nebulizer |
| DRUG | Nebuliser Suspension | 2% lidocaine dosed at 2 mg/kg (max 160 mg) applied via vibrating mesh nebulizer |
Timeline
- Start date
- 2019-04-01
- Primary completion
- 2020-08-31
- Completion
- 2020-08-31
- First posted
- 2019-02-04
- Last updated
- 2021-10-12
- Results posted
- 2021-10-12
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03829618. Inclusion in this directory is not an endorsement.