International Study of Cerebral Oxygenation and Electrical Activity During Major Neonatal Surgery

Sponsor
Children's Hospital of Philadelphia (Other)
Overall Status
Recruiting
CT.gov ID
NCT05673499
Collaborator
Masimo Corporation (Industry)
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Study Details

Study Description

Brief Summary

The goal of this observational study is to determine the incidence of perioperative cerebral desaturation in neonates undergoing surgery for congenital malformations. The main questions it aims to answer are:

  1. The perioperative factors associated with occurrence of cerebral desaturation

  2. The association between perioperative cerebral desaturation, perioperative/hospital outcomes, and physiological conditions.

Participants will undergo Near-infrared spectroscopy (NIRS) and electroencephalogram (EEG) monitoring for one hour before surgery, during surgery, and up to 24 hours after surgery.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The NIRS EEG sensors will be placed about an hour before surgery. The recording will start once sensors are placed, continue throughout the duration of surgery, and end 8-24 hours after end of surgery. Sensors will be removed at the end of recording. No additional anesthesia and/or sedation will be required for the preoperative and postoperative recordings. The EEG and NIRS monitors will be blinded to clinical staff. EEG and NIRS monitoring will not prolong anesthesia or the duration of the surgical repair, and should not interfere with routine patient care. NIRS and EEG data will be downloaded from the monitors at the end of recording for analysis.

    Medical record review will be conducted at 100 days postop or hospital discharge (whichever is sooner). The information below will be extracted:

    • Respiratory record

    • Post-op recovery, ICU, and discharge records

    • Cardiac and Neurologic records

    • Neurologic test such as radiology and lab tests

    • Mortality status

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    900 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    International Study of Cerebral Oxygenation and Electrical Activity During Major Neonatal Surgery
    Actual Study Start Date :
    Aug 12, 2022
    Anticipated Primary Completion Date :
    Dec 1, 2024
    Anticipated Study Completion Date :
    Dec 1, 2025

    Outcome Measures

    Primary Outcome Measures

    1. Percentage of participants with perioperative cerebral desaturation [24 hours]

      The incidence of cerebral desaturation in participants will be assessed by the Near-infrared Spectroscopy (NIRS) data recording of <70% and/or >10% decrease from baseline for > 3 minutes

    Secondary Outcome Measures

    1. Isoelectric EEG [up to 24 hours]

      Determined by EEG amplitude ≤ 10mV for ≥ 2 secs

    2. Perioperative outcomes [up to 100 days]

      Medical record review

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 60 Weeks
    Sexes Eligible for Study:
    All
    Inclusion Criteria:
    1. Infants ≤ 60 weeks post-menstrual age on day of surgery.

    2. Neonatal surgery for congenital abdominal/gastrointestinal malformations (diaphragmatic hernia, gastroschisis, omphalocele, intestinal atresia, Hirschsprung's disease, imperforate anus, necrotizing enterocolitis), congenital cystic adenomatoid/pulmonary airway malformation (CCAM/CPAM), esophageal/tracheoesophageal fistula (EF/TEF), and spinal malformations (myelomeningocele, sacrococcygeal teratoma).

    3. The same patient may be enrolled multiple times for repeat or different procedures that meet the above criteria. These subjects will be counted more than once towards the enrollment goal.

    4. Parental/guardian permission.

    Exclusion Criteria:
    1. Patients with hydrocephalus limiting frontal-parietal brain volume, interventricular hemorrhage (grades 3 or 4), malformation or cerebral infarction of frontal-parietal brain.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Children's Hospital at Montefiore New York New York United States 10467
    2 Children's Hospital of Philadelphia Philadelphia Pennsylvania United States 19104
    3 Children's Medical Center Dallas Dallas Texas United States 75235
    4 Children's Memorial Hermann Hospital Houston Texas United States 77030
    5 Perth Children's Hospital Nedlands Australia
    6 Royal Children's Hospital Parkville Australia
    7 Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo São Paulo Brazil
    8 Guangzhou women and children's medical center Guangzhou China
    9 Shanghai Children's Medical Center Shanghai China
    10 Shengjing Hospital of China Medical University Shenyang China
    11 West China Hospital and West China Second University Hospital Sichuan China
    12 Centre Hospitalier Universitaire de Bordeaux, Hopital des enfants Bordeaux France
    13 Post Graduate Institute of Medical Education and Research Chandigarh India
    14 Christian Medical College Hospital Vellore India
    15 Great Ormond Street Hospital for Children London United Kingdom

    Sponsors and Collaborators

    • Children's Hospital of Philadelphia
    • Masimo Corporation

    Investigators

    • Principal Investigator: Ian Yuan, MD, Children's Hospital of Philadelphia

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Children's Hospital of Philadelphia
    ClinicalTrials.gov Identifier:
    NCT05673499
    Other Study ID Numbers:
    • 22-019679
    First Posted:
    Jan 6, 2023
    Last Update Posted:
    Jan 6, 2023
    Last Verified:
    Dec 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Children's Hospital of Philadelphia

    Study Results

    No Results Posted as of Jan 6, 2023