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NCT03829618 · ClinicalTrials.gov registry record · Phase 3

Lidocaine Administration During Flexible Bronchoscopy and Endobronchial Ultrasound

A Phase 3 study, sponsored by Milton S. Hershey Medical Center.

Terminated
Registry status
Phase 3
Development phase
29
Enrollment target

NCT03829618: Clinical Trial Phase 3 study, sponsored by Milton S. Hershey Medical Center.

NCT03829618 is a Phase 3 study that was terminated before completion, run by Milton S. Hershey Medical Center. The registered enrollment target is 29 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT03829618, a Phase 3 study, was terminated before completion, sponsored by Milton S. Hershey Medical Center.

TERMINATED
Registry status
Phase 3
Development phase
29 participants
Enrollment target

Study 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.

Primary Outcome

Number of coughs during procedure as defined by cough requiring stopping procedure or treatment by anesthesiologist with propofol or alfentanyl

Interventions

  • DRUG Topical lidocaine
  • DRUG Nebuliser solution
  • DRUG Nebuliser Suspension

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2019-04-01
Est. Completion 2020-08-31
Phase Phase 3
Milton S. Hershey Medical Center

396 total trials

Why NCT03829618 stopped before completion

NCT03829618 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 29 participants, a relatively small participant target, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 3 interventions - of which Topical lidocaine is the first listed.

NCT03829618 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03829618 about?

NCT03829618 is a clinical study titled "Lidocaine Administration During Flexible Bronchoscopy and Endobronchial Ultrasound". 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.

What is the current status of trial NCT03829618?

This trial is currently terminated. It is a Phase 3 study. The enrollment target is 29 participants. The study started on 2019-04-01. Estimated completion is 2020-08-31.

What interventions are being tested in trial NCT03829618?

The interventions under investigation include: Topical lidocaine (DRUG), Nebuliser solution (DRUG), Nebuliser Suspension (DRUG).

Who is sponsoring clinical trial NCT03829618?

This trial is sponsored by Milton S. Hershey Medical Center, which has 396 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03829618's enrollment target sits among peer trials

29 1933rd of 2000 higher than 66 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT03829618, the US trial registry maintained by the National Library of Medicine. NCT03829618 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.