Study Evaluating Whether the Bispectral Index Prevents Patients at Higher Risk From Being Awake During Surgery and Anesthesia

ClinicalTrials.gov ID: NCT00682825

Public ClinicalTrials.gov record NCT00682825. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

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ClinicalTrials.gov public records Last synced Jul 22, 2026, 3:51 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

BAG-RECALL Study: BIS or Anesthesia Gas to Reduce Explicit Recall

Study identification

NCT ID: NCT00682825
Recruitment status: Completed
Study type: Interventional
Phase: Phase 4
Lead sponsor: Washington University School of Medicine; Other
Enrollment: 6,000 participants

Conditions and interventions

Conditions

Explicit Recall of Intra-Operative Events

Interventions

Bispectral index protocol Behavioral
End tidal anesthetic gas-guided Behavioral

Behavioral

Eligibility (public fields only)

Age range: 18 Years and older
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Feb 29, 2008
Primary completion: Nov 30, 2010
Completion: Not listed
Last update posted: Jan 3, 2011

Started 2008

United States locations

U.S. sites: 2
U.S. states: 2
U.S. cities: 2

Facility	City	State	ZIP	Site status
University of Chicago	Chicago	Illinois	—	—
Washington University	St Louis	Missouri	63110	—

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT00682825, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Jan 3, 2011 · Synced Jul 22, 2026

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The complete protocol, eligibility criteria, and contact information for NCT00682825 live on ClinicalTrials.gov.

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