- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07577726
Prospective Observational Multimodal Neuromonitoring During High-Risk Adult Surgery
Prospective Observational Multimodal Neuromonitoring During High-Risk Adult Surgery: A Single-Center Cohort Study of Quantitative EEG, Noninvasive Intracranial Dynamics, and Perioperative Physiologic Correlates
연구 개요
상태
상세 설명
BACKGROUND: Patients undergoing major spine surgery, liver transplantation, on-pump cardiac surgery, major vascular surgery, major thoracic surgery, major abdominal surgery, and neurosurgical craniotomy are exposed to substantial perioperative physiologic stress, including hemodynamic instability, blood loss, cardiopulmonary bypass, and procedure-specific periods of altered cerebral perfusion. Quantitative electroencephalography and noninvasive assessments of intracranial dynamics may provide complementary information about brain state and cerebrovascular physiology during these high-risk operations. However, the relationships between monitor-derived features and intraoperative events - including hypotension, anesthetic transitions, major surgical events, and postoperative outcomes - remain incompletely characterized.
DESIGN: Single-center prospective observational cohort study at UT Southwestern Medical Center. SedLine quantitative EEG data are extracted from standard-of-care clinical monitoring for all enrolled subjects. Brain4Care (B4C) noninvasive intracranial dynamics monitoring may additionally be placed as a research device depending on study workflow, patient characteristics, technical feasibility, and clinical context. Either monitoring configuration - SedLine alone or SedLine combined with B4C - constitutes a complete and valid study encounter.
The Moberg Clinical Platform (Moberg Analytics; FDA-cleared multimodal data integration system) serves as the primary data acquisition hub where deployed in the operating room, aggregating synchronized high-resolution physiologic waveforms alongside SedLine and B4C outputs. Where Moberg is unavailable, hemodynamic and physiologic variables are collected retrospectively from the Epic intraoperative anesthesia record.
MONITORING MODALITIES:
Research device placed specifically for this study (where deployed):
- Brain4Care (B4C) extensometry: skull-mounted noninvasive sensor recording cranial compliance-related waveform morphology (P2/P1 ratio, Time to Peak).
Standard-of-care clinical data recorded for research purposes:
- SedLine (Masimo): 4-channel frontal quantitative EEG providing Patient State Index, Spectral Edge Frequency, and exportable raw EDF-format waveforms.
- Moberg Clinical Platform: multimodal physiologic waveform integration including arterial blood pressure, SpO2, ECG, ventilator-derived parameters, temperature, and EtCO2.
DATA MANAGEMENT: Subjects are assigned unique study identifiers. Direct identifiers are removed from analytic datasets. Research data are stored on secure, institutionally approved systems accessible only to IRB-authorized study personnel. De-identified data may be shared with qualified external collaborators under executed data use agreements.
연구 유형
등록 (추정된)
연락처 및 위치
연구 연락처
- 이름: Noah Jouett, DO, PhD
- 전화번호: 2147862783
- 이메일: Noah.Jouett@UTSouthwestern.edu
연구 장소
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Texas
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Dallas, Texas, 미국, 75390
- UT Southwestern Medical Center - Clements University Hospital
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수석 연구원:
- Noah Jouett, DO, PhD
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연락하다:
- Noah Jouett, DO, PhD
- 전화번호: 2147862783
- 이메일: Noah.Jouett@UTSouthwestern.edu
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부수사관:
- Ulrike Hoffmann, MD, PhD
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부수사관:
- Peiman Lahsaei, MD
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참여기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
샘플링 방법
연구 인구
설명
Inclusion Criteria:
- Age 18 years or older
- Scheduled to undergo major spine surgery, liver transplantation, on-pump cardiac surgery, major vascular surgery, major thoracic surgery, major abdominal surgery, or neurosurgical craniotomy at UT Southwestern Medical Center
- Able to provide informed consent (self or legally authorized representative when applicable)
- Safe and feasible placement of SedLine and/or Brain4Care monitoring as determined by the clinical and research teams
- Anticipated availability of perioperative clinical data needed for study analyses
Exclusion Criteria:
- Age younger than 18 years
- Prisoner status
- Pregnancy
- Unable to provide informed consent in English (consent documents available in English only)
- Declining participation
- Lack of subject or legally authorized representative consent when required
- Clinical condition preventing safe or feasible placement of study monitors (e.g., incompatible surgical field location, significant facial or scalp injury, open wounds at intended sensor placement site)
- Operative workflow or clinical urgency precluding reasonable completion of consent and monitor placement prior to start of surgery
- Anticipated clinical data capture insufficient for meaningful analysis
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
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High-Risk Surgical Patients
Adult patients age 18 years or older undergoing major spine surgery, liver transplantation, on-pump cardiac surgery, major vascular surgery, major thoracic surgery, major abdominal surgery, or neurosurgical craniotomy at UT Southwestern Medical Center.
All participants undergo SedLine qEEG data capture from existing standard-of-care clinical monitoring.
A subset additionally undergo B4C noninvasive intracranial dynamics monitoring as a research device.
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Proportion of enrolled cases with analyzable SedLine quantitative EEG (Patient State Index) recording during surgery
기간: Intraoperative period (duration of surgery, typically 2-12 hours)
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Percentage of total enrolled cases yielding analyzable SedLine Patient State Index (PSI) epochs during the intraoperative period.
Signal quality assessed by artifact burden and data completeness.
Reported as a single proportion (percentage of cases with analyzable PSI data) across surgical case types.
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Intraoperative period (duration of surgery, typically 2-12 hours)
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Proportion of enrolled cases with analyzable Brain4Care extensometry (P2/P1 ratio) recording during surgery
기간: Intraoperative period (duration of surgery, typically 2-12 hours)
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Percentage of total enrolled cases yielding analyzable Brain4Care (B4C) extensometry P2/P1 ratio epochs during the intraoperative period.
Signal quality assessed by artifact burden and adequate waveform morphology.
Reported as a single proportion (percentage of cases with analyzable B4C data) across surgical case types.
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Intraoperative period (duration of surgery, typically 2-12 hours)
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Correlation between SedLine Patient State Index and intraoperative mean arterial pressure
기간: Intraoperative period through 90 days post-surgery
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Spearman correlation coefficient between SedLine-derived Patient State Index (PSI) values and concurrently recorded intraoperative mean arterial pressure.
Secondary within-case correlation analyses with vasoactive drug administration epochs, anesthetic transitions, blood loss events, and major surgical epochs will also be reported as correlation coefficients.
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Intraoperative period through 90 days post-surgery
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Correlation between Brain4Care extensometry P2/P1 ratio and intraoperative mean arterial pressure
기간: Intraoperative period through 90 days post-surgery
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Spearman correlation coefficient between Brain4Care (B4C) extensometry-derived P2/P1 ratio values and concurrently recorded intraoperative mean arterial pressure.
Secondary within-case correlation analyses with vasoactive drug administration epochs, anesthetic transitions, blood loss events, and major surgical epochs will also be reported as correlation coefficients.
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Intraoperative period through 90 days post-surgery
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Incidence of postoperative delirium assessed by Confusion Assessment Method (CAM)
기간: In-hospital postoperative period (expected 2-14 days post-surgery)
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Rate of postoperative delirium as documented by Confusion Assessment Method (CAM) assessments in nursing records during the postoperative hospital stay, reported as incidence (percentage of enrolled patients with at least one positive CAM screen).
Secondary analyses will examine associations between intraoperative SedLine PSI or B4C P2/P1 ratio features and postoperative delirium occurrence.
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In-hospital postoperative period (expected 2-14 days post-surgery)
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Proportion of cases with computable cerebrovascular reactivity indices from Brain4Care extensometry and arterial blood pressure data
기간: Intraoperative period
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Percentage of enrolled cases in which cerebrovascular reactivity-related indices can be computed from acquired Brain4Care (B4C) extensometry waveforms and concurrent arterial blood pressure data, reported as a single proportion with characterization of index distributions across surgical populations.
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Intraoperative period
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Functional status at 90 days post-surgery assessed by modified Rankin Scale via medical record review
기간: 90 days post-surgery
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Functional and neurological status assessed by modified Rankin Scale (mRS) score via medical record review and/or structured contact at up to 90 days from date of surgery.
Reported as ordinal mRS score (0-6).
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90 days post-surgery
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공동 작업자 및 조사자
수사관
- 수석 연구원: Noah Jouett, DO, PhD, University of Texas Southwestern Medical Center
연구 기록 날짜
연구 주요 날짜
연구 시작 (추정된)
기본 완료 (추정된)
연구 완료 (추정된)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
키워드
추가 관련 MeSH 약관
기타 연구 ID 번호
- STU20260828
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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섬망 상태에 대한 임상 시험
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Bozok University모병수술 후 합병증 | 소아 환자 | 수술 전 불안 (Ameliyat Öncesi Anksiyete) | Emergence Delirium (Derlenme Deliryumu)터키 (Türkiye)