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COMPLETED NA

Daily Sedative Interruption in Critically Ill Patients Being Managed With a Sedation Protocol.

NCT00675363 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine whether the use of both a nurse-driven sedation protocol and daily sedative interruption, compared with a sedation protocol alone, result in better outcomes for mechanically ventilated adults.

Conditions Studied

Interventions

  • PROCEDURE Protocolized Sedation
  • PROCEDURE Protocolized sedation, with daily interruption

Study Locations (16)

Ontario

  • Hamilton Health Sciences — Hamilton
  • St. Joesph's Healthcare — Hamilton
  • Sunnybrook HSC — Toronto
  • St. Michael's Hospital — Toronto
  • Mount Sinai Hospital — Toronto
  • Toronto General Hospital — Toronto
  • Toronto Western Hospital — Toronto

British Columbia

  • Royal Columbian Hospital — New Westminster
  • Surrey Memorial Hospital — Vancouver
  • Providence Health Care-St. Paul's Hospital — Vancouver

Alberta

  • Royal Alexandra Hospital — Edmonton
  • Walter C. Mackenzie Health Sciences Centre — Edmonton

California

  • Long Beach Memorial Medical Center — Long Beach

Massachusetts

  • Tuft's Medical Centre — Boston

Manitoba

  • Winnipeg Health Sciences Centre — Winnipeg

Quebec

  • Maisonneuve Rosemount — Montreal

Trial Details

FieldValue
Enrollment Target 410 participants
Start Date 2008-01
Est. Completion 2012-10-17
Phase NA

Sponsor

Mount Sinai Hospital, Canada

33 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00675363

The ClinicalTrials.gov registry entry for NCT00675363 describes a study currently listed as completed. It is categorized as NA, 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 410 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Mount Sinai Hospital, Canada, which has 33 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 Critical Illness appearing as the primary indexed condition, and to 2 interventions — of which Protocolized Sedation 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: NCT00675363 reports 16 study locations spanning 7 distinct geographic areas — top geographies include Ontario, British Columbia, Alberta. 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 NCT00675363 about?

NCT00675363 is a clinical study titled "Daily Sedative Interruption in Critically Ill Patients Being Managed With a Sedation Protocol.". The purpose of this study is to determine whether the use of both a nurse-driven sedation protocol and daily sedative interruption, compared with a sedation protocol alone, result in better outcomes for mechanically ventilated adults.

What is the current status of trial NCT00675363?

This trial is currently completed. It is a NA study. The enrollment target is 410 participants. The study started on 2008-01. Estimated completion is 2012-10-17.

What conditions does trial NCT00675363 study?

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

What interventions are being tested in trial NCT00675363?

The interventions under investigation include: Protocolized Sedation (PROCEDURE), Protocolized sedation, with daily interruption (PROCEDURE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00675363?

This trial is sponsored by Mount Sinai Hospital, Canada, which has 33 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00675363 being conducted?

This trial has 16 study locations across California, Massachusetts, Alberta, British Columbia, Manitoba. 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