Skip to content

Topical Anesthesia / Bronchoscopy

Topical Nasopharyngeal Anesthesia in Outpatient Bronchoscopy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02237651
Acronym
TNA
Enrollment
252
Registered
2014-09-11
Start date
2014-09-30
Completion date
2015-04-30
Last updated
2015-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Equally of Delivery Systems of Local Anesthesia in Bronchoscopy

Keywords

anesthesia, bronchosocopy, lung transplantation

Brief summary

The primary aim of this study is to compare a simplified single-use product (LMA® MAD Nasal™ Intranasal Mucosal Atomization Device, Teleflex medical, Kernen Germany) for topical nasopharyngeal anesthesia in comparison to a multi-use device (Laryngeal atomizer, Karl Storz, Tuttlingen, Germany in terms of patient self-rated nasopharyngeal symptoms.

Detailed description

Patients included in the first half of the study (topical anesthesia with the Laryngeal atomizer) and with need for another bronchoscopy in the second half of the study (topical anesthesia with the Intranasal Mucosal Atomization Device) will be asked to repeat the questionnaire after the second bronchoscopy to allow in-patient comparison. Description of the primary efficacy analysis and population: The primary endpoint of patient self-rated anesthesia by visual analogue scale after topical nasopharyngeal anesthesia for bronchoscopy.

Interventions

DEVICEtopical anesthesia multi-use device
DEVICEtopical anesthesia Intranasal Mucosal Atomization

Sponsors

Hannover Medical School
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 88 Years
Healthy volunteers
No

Inclusion criteria

* patients after lung transplantation (single, double or combined) * Informed consent * outpatient bronchoscopy

Exclusion criteria

* Oxygen requirement at rest * Need for peri-interventional sedation * limited German language skills or other reasons which might impair patient communication or computer handling

Design outcomes

Primary

MeasureTime frameDescription
Equally30 min.The primary endpoint of patient self-rated anesthesia by visual analogue scale after topical nasopharyngeal anesthesia for bronchoscopy.

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 2, 2026