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NCT04306211 · ClinicalTrials.gov registry record · NA

Comparison of Oxygenation Between Nasal PAP vs Nasal During Propofol-based Sedation for EUS

A NA study, sponsored by Indiana University.

Terminated
Registry status
NA
Development phase
11
Enrollment target

NCT04306211: Clinical Trial NA study, sponsored by Indiana University.

NCT04306211 is a NA study that was terminated before completion, run by Indiana University. The registered enrollment target is 11 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT04306211, a NA study, was terminated before completion, sponsored by Indiana University.

TERMINATED
Registry status
NA
Development phase
11 participants
Enrollment target

Study Summary

Randomized controlled single site study involves oxygenation, continuous positive airway pressure, and ventilation of subject via nasal mask and oxygenationvia closed facemask. The intervention of the study are delivery form of supplemental oxygen, bag-mask ventilation, and continuous nasal CPAP intraoperatively and in the post anesthesia care period.

Primary Outcome

Compare the incidence, duration, and severity of oxygen desaturation

Interventions

  • DEVICE SuperNO2VA

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2020-12-14
Est. Completion 2022-03-30
Phase NA
Indiana University

890 total trials

Why NCT04306211 stopped before completion

NCT04306211 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 11 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).

The record links to 0 conditions, and to 1 intervention - of which SuperNO2VA is the first listed.

NCT04306211 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04306211 about?

NCT04306211 is a clinical study titled "Comparison of Oxygenation Between Nasal PAP vs Nasal During Propofol-based Sedation for EUS". Randomized controlled single site study involves oxygenation, continuous positive airway pressure, and ventilation of subject via nasal mask and oxygenationvia closed facemask. The intervention of the study are delivery form of supplemental oxygen, bag-mask ventilation, and continuous nasal CPAP int...

What is the current status of trial NCT04306211?

This trial is currently terminated. It is a NA study. The enrollment target is 11 participants. The study started on 2020-12-14. Estimated completion is 2022-03-30.

What interventions are being tested in trial NCT04306211?

The interventions under investigation include: SuperNO2VA (DEVICE).

Who is sponsoring clinical trial NCT04306211?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04306211's enrollment target sits among peer trials

11 1927th of 2000 higher than 74 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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 NCT04306211, the US trial registry maintained by the National Library of Medicine. NCT04306211 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.