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NCT02908464 · ClinicalTrials.gov registry record · NA
Prevention of Early Postoperative Decline
A NA study of Delirium and Postoperative Cognitive Dysfunction, sponsored by Beth Israel Deaconess Medical Center.
- Completed
- Registry status
- NA
- Development phase
- 45
- Enrollment target
- 1
- Study location
NCT02908464 is a NA study of Delirium and Postoperative Cognitive Dysfunction that has completed, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 45 participants, below the 887-participant average among 62 other Delirium trials with a reported enrollment target (95% lower). The trial reports 1 study location across 1 state.
The verdict
NCT02908464, a NA study of Delirium and Postoperative Cognitive Dysfunction, has completed, sponsored by Beth Israel Deaconess Medical Center.
- COMPLETED
- Registry status
- NA
- Development phase
- 45 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this trial is to determine whether using a brain training program in the time leading up to as well as after heart surgery will reduce confusion and cognitive loss that can occur after surgery.
Conditions Studied
Interventions
- DEVICE Lumosity
Study Locations (1)
Massachusetts
- Beth Israel Deaconess Medical Center - Boston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 45 participants |
| Start Date | 2016-11 |
| Est. Completion | 2019-09 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02908464
The ClinicalTrials.gov registry entry for NCT02908464 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 45 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 887-participant average among 62 other Delirium trials with a reported enrollment target (95% lower). The listed sponsor is Beth Israel Deaconess Medical Center, which has 488 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Delirium appearing as the primary indexed condition, and to 1 intervention - of which Lumosity is the first listed.
NCT02908464 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.
Frequently Asked Questions
What is clinical trial NCT02908464 about?
NCT02908464 is a clinical study titled "Prevention of Early Postoperative Decline". The purpose of this trial is to determine whether using a brain training program in the time leading up to as well as after heart surgery will reduce confusion and cognitive loss that can occur after surgery.
What is the current status of trial NCT02908464?
This trial is currently completed. It is a NA study. The enrollment target is 45 participants. The study started on 2016-11. Estimated completion is 2019-09.
What conditions does trial NCT02908464 study?
This clinical trial studies the following conditions: Delirium, Postoperative Cognitive Dysfunction.
What interventions are being tested in trial NCT02908464?
The interventions under investigation include: Lumosity (DEVICE).
Who is sponsoring clinical trial NCT02908464?
This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02908464 being conducted?
This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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Related
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