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COMPLETED Phase 4

Moderate Versus Deep Procedural Sedation With Propofol in the Emergency Department

NCT02404610 · View on ClinicalTrials.gov ↗

Study Summary

This study is a clinical trial of moderate sedation versus deep sedation with propofol for procedural sedation in the Emergency Department. The purpose of this study is to compare the rate of amnesia and respiratory depression rate in patients who receive moderate sedation to those that receive deep sedation.

Conditions Studied

Interventions

  • PROCEDURE Moderate Procedural Sedation with a sedative medication.
  • PROCEDURE Deep Procedural Sedation with a sedative medication.
  • DRUG propofol

Study Locations (1)

Minnesota

  • Hennepin County Medical Center — Minneapolis

Trial Details

FieldValue
Enrollment Target 107 participants
Start Date 2014-07
Est. Completion 2018-12-01
Phase Phase 4

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02404610

The ClinicalTrials.gov registry entry for NCT02404610 describes a study currently listed as completed. It is categorized as Phase 4, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 107 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Hennepin Healthcare Research Institute, which has 74 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Pain appearing as the primary indexed condition, and to 3 interventions — of which Moderate Procedural Sedation with a sedative medication. is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02404610 reports 1 study location spanning 1 distinct geographic area — top geographies include Minnesota. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02404610 about?

NCT02404610 is a clinical study titled "Moderate Versus Deep Procedural Sedation With Propofol in the Emergency Department". This study is a clinical trial of moderate sedation versus deep sedation with propofol for procedural sedation in the Emergency Department. The purpose of this study is to compare the rate of amnesia and respiratory depression rate in patients who receive moderate sedation to those that receive deep...

What is the current status of trial NCT02404610?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 107 participants. The study started on 2014-07. Estimated completion is 2018-12-01.

What conditions does trial NCT02404610 study?

This clinical trial studies the following conditions: Pain. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02404610?

The interventions under investigation include: Moderate Procedural Sedation with a sedative medication. (PROCEDURE), Deep Procedural Sedation with a sedative medication. (PROCEDURE), propofol (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02404610?

This trial is sponsored by Hennepin Healthcare Research Institute, which has 74 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02404610 being conducted?

This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial