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Postoperative Neurocognitive Disorders

Mechanisms Mediating Postoperative Neurocognitive Disorders

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04244162
Acronym
PNCD
Enrollment
32
Registered
2020-01-28
Start date
2020-12-12
Completion date
2025-08-31
Last updated
2025-11-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obstructive Sleep Apnea, Neurocognitive Disorders

Keywords

brain imaging, neurocognitive testing

Brief summary

The purpose of this study is to examine the mechanisms of brain injury contributing to postoperative neurocognitive disorders (PNCD) in an at-risk population (obstructive sleep apnea (OSA)) undergoing surgery. The investigators will enroll 50 OSA patients scheduled for surgery. All patients will have a brain scan (fMRI) within five days before surgery and two days and six months after surgery. During this visit cognitive function will be assessed using the Wide Range Assessment of Memory and Learning (WRAML2) and Montreal Cognitive Assessment (MoCA) tests. Patients will also be asked to participate in a blood draw during the first 2 visits for fMRI (within five days of surgery and two days after surgery). The Confusion Assessment Method (CAM-S) test, will be used to examine postoperative delirium.

Detailed description

The investigators will examine the potential mechanisms of brain injury contributing to postoperative neurocognitive disorders (PNCD) in an at-risk population (obstructive sleep apnea (OSA)). This study proposes that neuro-inflammation is associated with measurable tissue changes that can be examined with MD measures and blood biomarkers. On the day of surgery, standard of care procedures will take place. Hemodynamic vitals will be continuously monitored. As per the latest guidelines and recommendations from the American Society of Anesthesiologists (ASA), mean arterial pressure (MAP) will be targeted to \> 60 mmHg or within 20% of baseline values, and processed EEG-guided anesthesia will be monitored to maintain a patient state index between 20-50. Electronic medical records and intraoperative integrated physiologic waveform will be collected. In summary, the investigators will examine the potential mechanisms of brain injury contributing to postoperative delirium (POD) and acute and long-lasting neurocognitive deficits in an at-risk population (OSA).

Interventions

DIAGNOSTIC_TESTBrain Imaging

Magnetic resonance imaging (MRI) using diffusion tensor imaging (DTI)-based mean diffusivity (MD) measures.

DIAGNOSTIC_TESTCognitive testing

Wide Range Assessment of Memory and Learning (WRAML2), Montreal Cognitive Assessment (MoCA), and Confusion Assessment Method for the ICU -severity (CAM-ICU S) tests.

DIAGNOSTIC_TESTBlood Biomarkers

Inflammatory markers

Sponsors

Massachusetts General Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

Subjects with a diagnosis of moderate-to-severe OSA (apnea hypopnea index \[AHI\]\>15 events/hour confirmed by overnight polysomnography), scheduled for open or robotic surgery (abdominal, gynecologic, or urologic), and upper or lower extremity orthopedic procedures

Design outcomes

Primary

MeasureTime frameDescription
Postoperative DeliriumA two times per day for up to three days or discharge from the hospital.The Confusion Assessment Method (CAM-S) test
Postoperative cognitive dysfunction - delayed cognitive recoveryPost-surgery (within two days post surgery).Montreal Cognitive Assessment (MoCA) test
Postoperative cognitive dysfunction - neurocognitive disorderPost-surgery (6 months after surgery).Montreal Cognitive Assessment (MoCA) test
Preoperative cognitive function IIpre-surgery (within five days before surgery)Wide Range Assessment of Memory and Learning (WRAML2)
Postoperative cognitive dysfunction - delayed cognitive recovery IIPost-surgery (within two days post surgery).Wide Range Assessment of Memory and Learning (WRAML2)
Postoperative cognitive dysfunction - neurocognitive disorder IIPost-surgery (6 months after surgery).Wide Range Assessment of Memory and Learning (WRAML2)
Preoperative cognitive functionpre-surgery (within five days before)Montreal Cognitive Assessment (MoCA) test

Secondary

MeasureTime frameDescription
Blood Serum anti-inflammatory Biomarkers IIpost-surgery (within two days of surgery).Assess blood inflammatory biomarkers (IL6, TNFa and IL1B) using enzyme-linked immunosorbent assay
Brain changespre- (within five days before) and post-surgery (within two days and 6 months).Using non-invasive magnetic resonance imaging based diffusion tensor imaging
Brain changes IIPost-surgery (within two days post surgery).Using non-invasive magnetic resonance imaging based diffusion tensor imaging
Brain changes IIIPost-surgery (within six months post surgery).Using non-invasive magnetic resonance imaging based diffusion tensor imaging
Blood Serum anti-inflammatory Biomarkerspre- (within five days before surgery)Assess blood inflammatory biomarkers (IL6, TNFa and IL1B) using enzyme-linked immunosorbent assay

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026