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Individual Cerebral Hemodynamic Oxygenation Relationships

NCT04435834 · Status: RECRUITING · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2024-09-03

No results posted yet for this study

Summary

This is a randomized controlled trial in patients who require clinical anesthesia. The main purpose of this study is to understand whether there are differences in the cerebral blood flow, and oxygen metabolism affected by two types of anesthesia: propofol or sevoflurane. Subjects who require clinical anesthesia for a clinical MRI and for whom the use of propofol and sevoflurane are in clinical equipoise will be offered to have the anesthesia they will receive during their MRI randomized. All eligible subjects will be asked to provide informed consent before participating in the study.

Conditions

  • Anesthesia
  • Anesthesia; Reaction

Interventions

DRUG

Propofol or Sevoflurane

Patient's will be randomized to the group receiving propofol, or the group receiving sevoflurane.

Sponsors & Collaborators

  • Matthew Borzage

    lead OTHER

Principal Investigators

  • Matthew Borzage, PhD · Children's Hospital Los Angeles

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
DOUBLE
Model
PARALLEL

Eligibility

Max Age
1 Year
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-06-09
Primary Completion
2026-09-10
Completion
2026-09-10
FDA Drug
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04435834 on ClinicalTrials.gov