Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT02650687 · ClinicalTrials.gov registry record
Optimizing Postoperative Cognition the Elderly
A clinical trial of Postoperative Cognitive Dysfunction and POCD, sponsored by Icahn School of Medicine at Mount Sinai.
- Completed
- Registry status
- 178
- Enrollment target
- 1
- Study location
NCT02650687: Completed study of Postoperative Cognitive Dysfunction and POCD, sponsored by Icahn School of Medicine at Mount Sinai.
NCT02650687 is a study of Postoperative Cognitive Dysfunction and POCD that has completed, run by Icahn School of Medicine at Mount Sinai. The registered enrollment target is 178 participants, roughly in line with the 166-participant average among 6 other Postoperative Cognitive Dysfunction trials with a reported enrollment target. The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02650687, a study of Postoperative Cognitive Dysfunction and POCD, has completed, sponsored by Icahn School of Medicine at Mount Sinai.
- COMPLETED
- Registry status
- 178 participants
- Enrollment target
- 1
- Study location
Study Summary
This study will recruit surgical patients more than 65 years old. Patients who participate will wear a sticker on their forehead during surgery which monitors their brain waves (electroencephalogram, EEG) and participate in memory testing before and after surgery. Brain wave patterns will be compared between patients who have problems with memory and thinking after surgery and those who do not. The hypothesis is that there will be characteristic brain wave patients for who will go on to have problems with memory and thinking after surgery.
Primary Outcome
Postoperative Cognitive Dysfunction - UDS battery is the standard ADRC neuropsychological battery and will be used to measure cognition
Conditions Studied
Interventions
- PROCEDURE Processed EEG
Study Locations (1)
New York
- Icahn School of Medicine at Mount Sinai - New York
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 178 participants |
| Start Date | 2015-10 |
| Est. Completion | 2019-11-14 |
What the finished NCT02650687 record still lists
NCT02650687 is an observational study that tracks outcomes without assigning an intervention. The registered 178 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 166-participant average among 6 other Postoperative Cognitive Dysfunction trials with a reported enrollment target.
The record links to 2 conditions, with Postoperative Cognitive Dysfunction appearing as the primary indexed condition, and to 1 intervention - of which Processed EEG is the first listed.
NCT02650687 reports a single indexed study location in New York.
Frequently Asked Questions
What is clinical trial NCT02650687 about?
NCT02650687 is a clinical study titled "Optimizing Postoperative Cognition the Elderly". This study will recruit surgical patients more than 65 years old. Patients who participate will wear a sticker on their forehead during surgery which monitors their brain waves (electroencephalogram, EEG) and participate in memory testing before and after surgery. Brain wave patterns will be compare...
What is the current status of trial NCT02650687?
This trial is currently completed. The enrollment target is 178 participants. The study started on 2015-10. Estimated completion is 2019-11-14.
What conditions does trial NCT02650687 study?
This clinical trial studies the following conditions: Postoperative Cognitive Dysfunction, POCD.
What interventions are being tested in trial NCT02650687?
The interventions under investigation include: Processed EEG (PROCEDURE).
Who is sponsoring clinical trial NCT02650687?
This trial is sponsored by Icahn School of Medicine at Mount Sinai, which has 708 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02650687 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Postoperative Cognitive Dysfunction
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
CEReBral AutorEgulation in Non-cardiac SuRgery and Relationship to Postoperative DeliriUm State
RECRUITING
-
The Caffeine, Postoperative Delirium, and Change in Outcomes After Surgery (CAPACHINOS-2) Study
RECRUITING · Phase 2
-
Kids With Iron Deficiency and Scoliosis
RECRUITING · NA
-
Total Intravenous Versus Inhalational Anesthesia- A Geriatric Anesthesia Study
RECRUITING · Phase 4
-
Effects of Brain Beta-Amyloid on Postoperative Cognition
ACTIVE NOT RECRUITING · Phase 4
-
Prevention of Early Postoperative Decline
COMPLETED · NA
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT03642002 · 178 participants · NA
The Effects of Music Therapy on Adult Patients Requiring Mechanical Ventilation in the ICU
- NCT04227847 · 178 participants · Phase 1
A Safety Study of SEA-CD70 in Patients With Myeloid Malignancies
- NCT04855214 · 178 participants
Evaluating the Experience of Upper Limb Prosthesis Use
- NCT05391126 · 178 participants · NA
GENOCARE: A Prospective, Randomized Clinical Trial of Genotype-Guided Dosing Versus Usual Care
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia