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NCT02728726 · ClinicalTrials.gov registry record · Phase 4

Sugammadex vs Placebo to Prevent Residual Neuromuscular Block

A Phase 4 study, sponsored by Mayo Clinic.

Completed
Registry status
Phase 4
Development phase
260
Enrollment target

NCT02728726: Completed Phase 4 study, sponsored by Mayo Clinic.

NCT02728726 is a Phase 4 study that has completed, run by Mayo Clinic. The registered enrollment target is 260 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (50% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

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The verdict

NCT02728726, a Phase 4 study, has completed, sponsored by Mayo Clinic.

COMPLETED
Registry status
Phase 4
Development phase
260 participants
Enrollment target

Study Summary

The study is designed to determine whether patients who receive sugammadex immediately after tracheal extubation will exhibit a decrease in the incidence of postoperative residual paralysis and an associated decrease in the incidence of postoperative respiratory depression.

Primary Outcome

The number of subjects who have a MV as defined as \[MV \<80% MV predicted (MVPRED) based on Body Surface Area\]. MV (or respiratory minute volume or minute volume) is the volume of gas inhaled (inhaled minute volume) or exhaled (exhaled minute volume) from a person's lungs per minute.

Interventions

  • DRUG Placebo
  • DRUG Sugammadex

Trial Details

FieldValue
Enrollment Target 260 participants
Start Date 2016-06
Est. Completion 2019-12
Phase Phase 4
Mayo Clinic

2,844 total trials

What the finished NCT02728726 record still lists

NCT02728726 is an interventional study that assigns participants to a tested intervention. The registered 260 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (50% lower).

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

NCT02728726 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02728726 about?

NCT02728726 is a clinical study titled "Sugammadex vs Placebo to Prevent Residual Neuromuscular Block". The study is designed to determine whether patients who receive sugammadex immediately after tracheal extubation will exhibit a decrease in the incidence of postoperative residual paralysis and an associated decrease in the incidence of postoperative respiratory depression.

What is the current status of trial NCT02728726?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 260 participants. The study started on 2016-06. Estimated completion is 2019-12.

What interventions are being tested in trial NCT02728726?

The interventions under investigation include: Placebo (DRUG), Sugammadex (DRUG).

Who is sponsoring clinical trial NCT02728726?

This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02728726's enrollment target sits among peer trials

260 326th of 2000 higher than 1,670 of 2,000 other Phase 4 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 4 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 NCT02728726, the US trial registry maintained by the National Library of Medicine. NCT02728726 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.