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NCT02918877 · ClinicalTrials.gov registry record · Phase 1

Anesthetics to Prevent Lung Injury in Cardiac Surgery

A Phase 1 study, sponsored by Beth Israel Deaconess Medical Center.

Completed
Registry status
Phase 1
Development phase
51
Enrollment target

NCT02918877: Completed Phase 1 study, sponsored by Beth Israel Deaconess Medical Center.

NCT02918877 is a Phase 1 study that has completed, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 51 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (15% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02918877, a Phase 1 study, has completed, sponsored by Beth Israel Deaconess Medical Center.

COMPLETED
Registry status
Phase 1
Development phase
51 participants
Enrollment target

Study Summary

The purpose of this study is to investigate whether the use of inhaled anesthetics, compared to intravenous anesthetics, can affect the amount of lung inflammation and postoperative respiratory complications seen after cardiac surgery.

Primary Outcome

Inflammatory mediator found in BAL fluid during lung inflammation

Interventions

  • DRUG Sevoflurane
  • DRUG Propofol

Trial Details

FieldValue
Enrollment Target 51 participants
Start Date 2017-06-09
Est. Completion 2021-02-01
Phase Phase 1

What the finished NCT02918877 record still lists

NCT02918877 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 51 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (15% lower).

The record links to 0 conditions, and to 2 interventions - of which Sevoflurane is the first listed.

NCT02918877 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02918877 about?

NCT02918877 is a clinical study titled "Anesthetics to Prevent Lung Injury in Cardiac Surgery". The purpose of this study is to investigate whether the use of inhaled anesthetics, compared to intravenous anesthetics, can affect the amount of lung inflammation and postoperative respiratory complications seen after cardiac surgery.

What is the current status of trial NCT02918877?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 51 participants. The study started on 2017-06-09. Estimated completion is 2021-02-01.

What interventions are being tested in trial NCT02918877?

The interventions under investigation include: Sevoflurane (DRUG), Propofol (DRUG).

Who is sponsoring clinical trial NCT02918877?

This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02918877's enrollment target sits among peer trials

51 969th of 2000 higher than 1,028 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT02918877, the US trial registry maintained by the National Library of Medicine. NCT02918877 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.