Relationship Between Intracranial Blood Flow and Peripheral Perfusion in Patients With Craniocerebral Injury

Sponsor
Peking Union Medical College Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT06016751
Collaborator
(none)
30
1
12
2.5

Study Details

Study Description

Brief Summary

Neurocritical care is a major branch in the field of critical care medicine, and more than 50% of the neurocritical care patients in the Tibet Autonomous Region People's Hospital (TARPH) are in neurocritical care, of which cranial damage accounts for about 30%, and paroxysmal sympathetic hyperexcitability syndrome (PSH) after traumatic brain injury(TBI)is a common complication, which affects the cardiorespiratory and cerebral functions to varying degrees, and optimizing the cerebral perfusion and oxygenation supply is the key point in the treatment of TIB, and the maintenance of the cerebral homeostasis and the functional homeostasis is currently an international hotspot for treatment. Maintaining cerebral homeostasis and body function homeostasis is an international hotspot in the treatment of TIB. This study intends to elaborate on the relationship between PSH and Intracranial blood flow in patients with TBI, as well as the effect of anti-stress treatment on Intracranial blood flow. Implementation Patients with brain injury admitted to our department from January 2021 to January 2022 were included. Non-invasive transcranial Doppler ultrasound was applied to measure cerebral blood flow, non-invasive local cerebral oxygen saturation monitor to measure local cerebral oxygen saturation, and an electroencephalography bispectrometer to measure BIS score to quantify the depth of sedation during the experimental process. Bedside ultrasound monitored the right heart function and lung water status, and the data of each monitoring index were monitored and recorded throughout the whole process, and the relationship between concomitant PSH and Intracranial blood flow in TBI patients was found according to the statistical analysis. Ultimately, to achieve the control of TBI complications and improve patient rescue. To expect to achieve the purpose of improving the prognosis of TBI patients.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    30 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Relationship Between Intracranial Blood Flow and Peripheral Perfusion in Patients With Craniocerebral Injury Assessed by Doppler Ultrasound and Prognostic Assessment
    Actual Study Start Date :
    Jan 1, 2021
    Actual Primary Completion Date :
    Jan 1, 2022
    Actual Study Completion Date :
    Jan 1, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    cranial damage

    Our study was a prospective observational study which included only a group of patients who were diagnosed with acute craniocerebral injury.

    Outcome Measures

    Primary Outcome Measures

    1. intracranial blood flow [Day 1,Day 3,Day 5]

      Mean intracranial middle cerebral artery blood flow velocity and pulsatility index measured using ultrasound Doppler in enrolled patients.

    2. Paroxysmal sympathetic excitation [Day 1,Day 3,Day 5]

      Use of the Paroxysmal Sympathetic Nerve Score to assess paroxysmal sympathoexcitatory performance in patients.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Craniocerebral injury patients;

    • The middle cerebral artery blood flow spectrum can be clearly displayed with a bedside TCD;

    Exclusion Criteria:
    • Age Under 18 years;

    • history of cardiovascular disease such as coronary artery disease, heart failure, or atrial fibrillation;

    • presence of severe valvular disease or ejection fraction (EF) <30%;

    • chronic lung disease;

    • chronic liver failure or renal insufficiency;

    • persons with co-morbidities of malignant neoplasms;

    • persons who had co-morbidities with acute and chronic infectious diseases prior to craniocerebral injuries;

    • women who were pregnant and breastfeeding;

    • history of psychiatric disorders;

    • history of drug abuse or alcohol misuse;

    • history of β-blockers;

    • co-morbidities with spinal cord injuries; and persons who had died or been discharged from hospital within 1 week of hospitalization or who had not been able to obtain a clear image with ultrasonography.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Wei Du Beijing Beijing China

    Sponsors and Collaborators

    • Peking Union Medical College Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Peking Union Medical College Hospital
    ClinicalTrials.gov Identifier:
    NCT06016751
    Other Study ID Numbers:
    • YLong
    First Posted:
    Aug 30, 2023
    Last Update Posted:
    Aug 30, 2023
    Last Verified:
    Aug 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 30, 2023